13-53035624-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53035624
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 53035624
    reference: chr 13
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000136108
  ensembl protein: ENSP00000367276
  ensembl transcript: ENST00000378037
  gene symbol: CKAP2
  hgvsc: ENST00000378037.5:c.666C>T
  hgvsp: ENST00000378037.5:c.666C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1990
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136108
  ensembl protein: ENSP00000367273
  ensembl transcript: ENST00000378034
  gene symbol: CKAP2
  hgvsc: ENST00000378034.3:c.663C>T
  hgvsp: ENST00000378034.3:c.663C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1990
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136108
  ensembl protein: ENSP00000258607
  ensembl transcript: ENST00000258607
  gene symbol: CKAP2
  hgvsc: ENST00000258607.5:c.663C>T
  hgvsp: ENST00000258607.5:c.663C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1990
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136108
  ensembl protein: ENSP00000417830
  ensembl transcript: ENST00000490903
  gene symbol: CKAP2
  hgvsc: ENST00000490903.1:c.519C>T
  hgvsp: ENST00000490903.1:c.519C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1990
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2053
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31944
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6749
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14843
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1068
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3424
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8384
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2697
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4031
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asn222Asn
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

11-124746272-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124746272
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124746272
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 3802
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2629G>T
  hgvsp: ENSP00000441797.1:p.Ala877Ser
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.256G>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2695G>T
  hgvsp: ENSP00000380903.1:p.Ala899Ser
  variant of: http://identifiers.org/hgnc/13433
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31243
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8423
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27876
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1038
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 558
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 966
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3975
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6540
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ala899Ser
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

11-124746274-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124746274
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124746274
    reference: chr 11
allele count: 3
allele frequency: 7.684426229508197e-4
allele num: 3904
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2631A>G
  hgvsp: ENST00000538940.1:c.2631A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2697A>G
  hgvsp: ENST00000397801.1:c.2697A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.258A>G
  variant of: http://identifiers.org/hgnc/13433
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8259
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31454
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3636
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 634
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28256
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6604
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 862
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1025
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 2
hgvs: p.Ala899Ala
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

11-124746276-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124746276
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124746276
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 3794
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2633C>T
  hgvsp: ENSP00000441797.1:p.Ala878Val
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.260C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2699C>T
  hgvsp: ENSP00000380903.1:p.Ala900Val
  variant of: http://identifiers.org/hgnc/13433
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31419
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7960
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1055
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 653
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4000
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 989
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6171
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27784
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.75e1
  variant carriers: 1
hgvs: p.Ala900Val
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

11-124746279-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124746279
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124746279
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 3664
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2702G>A
  hgvsp: ENSP00000380903.1:p.Cys901Tyr
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.263G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2636G>A
  hgvsp: ENSP00000441797.1:p.Cys879Tyr
  variant of: http://identifiers.org/hgnc/13433
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7728
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31480
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27655
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 998
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1087
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 703
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5917
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4075
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Cys901Tyr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

11-124746280-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124746280
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124746280
    reference: chr 11
allele count: 1
allele frequency: 2.724795640326976e-4
allele num: 3670
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.264C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2637C>T
  hgvsp: ENST00000538940.1:c.2637C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2703C>T
  hgvsp: ENST00000397801.1:c.2703C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13433
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7684
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31583
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5963
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 979
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4029
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 727
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 958
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27910
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Cys901Cys
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

11-124746282-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124746282
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124746282
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 3884
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.266G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2705G>A
  hgvsp: ENSP00000380903.1:p.Gly902Glu
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2639G>A
  hgvsp: ENSP00000441797.1:p.Gly880Glu
  variant of: http://identifiers.org/hgnc/13433
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31809
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7587
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 820
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3643
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 906
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 868
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28349
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6136
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gly902Glu
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: DP
site quality: InbreedingCoeff

11-124746283-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124746283
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124746283
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 3864
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.267G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2706G>A
  hgvsp: ENST00000397801.1:c.2706G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2640G>A
  hgvsp: ENST00000538940.1:c.2640G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13433
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7518
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31822
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 884
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6083
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28294
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3656
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 836
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 906
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gly902Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

13-53035625-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53035625
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 53035625
    reference: chr 13
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136108
  ensembl protein: ENSP00000367276
  ensembl transcript: ENST00000378037
  gene symbol: CKAP2
  hgvsc: ENST00000378037.5:c.667A>G
  hgvsp: ENSP00000367276.4:p.Thr223Ala
  variant of: http://identifiers.org/hgnc/1990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136108
  ensembl protein: ENSP00000367273
  ensembl transcript: ENST00000378034
  gene symbol: CKAP2
  hgvsc: ENST00000378034.3:c.664A>G
  hgvsp: ENSP00000367273.2:p.Thr222Ala
  variant of: http://identifiers.org/hgnc/1990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136108
  ensembl protein: ENSP00000258607
  ensembl transcript: ENST00000258607
  gene symbol: CKAP2
  hgvsc: ENST00000258607.5:c.664A>G
  hgvsp: ENSP00000258607.5:p.Thr222Ala
  variant of: http://identifiers.org/hgnc/1990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136108
  ensembl protein: ENSP00000417830
  ensembl transcript: ENST00000490903
  gene symbol: CKAP2
  hgvsc: ENST00000490903.1:c.520A>G
  hgvsp: ENSP00000417830.1:p.Thr174Ala
  variant of: http://identifiers.org/hgnc/1990
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2058
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14845
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31932
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6751
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34313
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3426
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4030
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8392
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2699
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Thr223Ala
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

13-53035633-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53035633
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 53035633
    reference: chr 13
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136108
  ensembl protein: ENSP00000367276
  ensembl transcript: ENST00000378037
  gene symbol: CKAP2
  hgvsc: ENST00000378037.5:c.675T>A
  hgvsp: ENSP00000367276.4:p.Ser225Arg
  variant of: http://identifiers.org/hgnc/1990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136108
  ensembl protein: ENSP00000417830
  ensembl transcript: ENST00000490903
  gene symbol: CKAP2
  hgvsc: ENST00000490903.1:c.528T>A
  hgvsp: ENSP00000417830.1:p.Ser176Arg
  variant of: http://identifiers.org/hgnc/1990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136108
  ensembl protein: ENSP00000258607
  ensembl transcript: ENST00000258607
  gene symbol: CKAP2
  hgvsc: ENST00000258607.5:c.672T>A
  hgvsp: ENSP00000258607.5:p.Ser224Arg
  variant of: http://identifiers.org/hgnc/1990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136108
  ensembl protein: ENSP00000367273
  ensembl transcript: ENST00000378034
  gene symbol: CKAP2
  hgvsc: ENST00000378034.3:c.672T>A
  hgvsp: ENSP00000367273.2:p.Ser224Arg
  variant of: http://identifiers.org/hgnc/1990
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31875
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6783
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14832
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4039
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5281
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3439
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8392
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1156
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ser225Arg
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: T
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum

13-53035634-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 53035634
    reference: chr 13
  end: Position
    type: ExactPosition
    position: 53035634
    reference: chr 13
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136108
  ensembl protein: ENSP00000258607
  ensembl transcript: ENST00000258607
  gene symbol: CKAP2
  hgvsc: ENST00000258607.5:c.673G>T
  hgvsp: ENSP00000258607.5:p.Val225Leu
  variant of: http://identifiers.org/hgnc/1990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136108
  ensembl protein: ENSP00000367273
  ensembl transcript: ENST00000378034
  gene symbol: CKAP2
  hgvsc: ENST00000378034.3:c.673G>T
  hgvsp: ENSP00000367273.2:p.Val225Leu
  variant of: http://identifiers.org/hgnc/1990
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136108
  ensembl protein: ENSP00000367276
  ensembl transcript: ENST00000378037
  gene symbol: CKAP2
  hgvsc: ENST00000378037.5:c.676G>T
  hgvsp: ENSP00000367276.4:p.Val226Leu
  variant of: http://identifiers.org/hgnc/1990
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136108
  ensembl protein: ENSP00000417830
  ensembl transcript: ENST00000490903
  gene symbol: CKAP2
  hgvsc: ENST00000490903.1:c.529G>T
  hgvsp: ENSP00000417830.1:p.Val177Leu
  variant of: http://identifiers.org/hgnc/1990
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31862
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6796
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2069
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14830
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1079
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34238
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5281
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1156
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2712
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3441
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Val226Leu
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD

11-124746284-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124746284
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124746284
    reference: chr 11
allele count: 3
allele frequency: 7.767995857068876e-4
allele num: 3862
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.268G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2641G>A
  hgvsp: ENSP00000441797.1:p.Ala881Thr
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2707G>A
  hgvsp: ENSP00000380903.1:p.Ala903Thr
  variant of: http://identifiers.org/hgnc/13433
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7523
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31814
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3518
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 879
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 865
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6113
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28420
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 855
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala903Thr
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

11-124746286-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124746286
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124746286
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 3856
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2709G>A
  hgvsp: ENST00000397801.1:c.2709G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2643G>A
  hgvsp: ENST00000538940.1:c.2643G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.270G>A
  variant of: http://identifiers.org/hgnc/13433
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7385
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31909
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3505
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 842
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28562
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 838
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 940
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6002
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
hgvs: p.Ala903Ala
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

11-124746303-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124746303
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124746303
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 4328
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2660G>C
  hgvsp: ENSP00000441797.1:p.Cys887Ser
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.287G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2726G>C
  hgvsp: ENSP00000380903.1:p.Cys909Ser
  variant of: http://identifiers.org/hgnc/13433
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6787
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32867
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 755
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1262
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3146
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29742
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5683
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 729
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Cys909Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

11-124746336-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124746336
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124746336
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 3794
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2759A>G
  hgvsp: ENSP00000380903.1:p.Lys920Arg
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2693A>G
  hgvsp: ENSP00000441797.1:p.Lys898Arg
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.320A>G
  variant of: http://identifiers.org/hgnc/13433
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6302
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34513
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32075
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 560
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 685
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2530
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5855
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Lys920Arg
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

11-124746340-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124746340
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124746340
    reference: chr 11
allele count: 1
allele frequency: 2.785515320334262e-4
allele num: 3590
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.324G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2697G>A
  hgvsp: ENST00000538940.1:c.2697G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2763G>A
  hgvsp: ENST00000397801.1:c.2763G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13433
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34463
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 783
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.75e1
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genotype quality: GenotypeQuality
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  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2892
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31727
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5531
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Glu921Glu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

11-124746340-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124746340
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124746340
    reference: chr 11
allele count: 1
allele frequency: 2.785515320334262e-4
allele num: 3590
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2763G>C
  hgvsp: ENSP00000380903.1:p.Glu921Asp
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2697G>C
  hgvsp: ENSP00000441797.1:p.Glu899Asp
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.324G>C
  variant of: http://identifiers.org/hgnc/13433
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6105
  bin: 7.5e0
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34463
  bin: 2.5e0
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 783
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2892
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 2.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 3.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 5531
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31727
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Glu921Asp
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: DP

11-124746348-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124746348
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124746348
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 3262
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2771A>T
  hgvsp: ENSP00000380903.1:p.His924Leu
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2705A>T
  hgvsp: ENSP00000441797.1:p.His902Leu
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.332A>T
  variant of: http://identifiers.org/hgnc/13433
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34628
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5775
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 596
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 672
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32017
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2755
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5343
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
hgvs: p.His924Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum

11-124746365-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124746365
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124746365
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 1924
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2779+9C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2713+9C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.340+9C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.4C>T
  variant of: http://identifiers.org/hgnc/13433
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 4750
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34750
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31653
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3309
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3726
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 848
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 686
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD

11-124746366-CG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124746366
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124746365
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 1834
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.7delG
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.3delG
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2713+12delG
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2779+12delG
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.340+12delG
  variant of: http://identifiers.org/hgnc/13433
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4731
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34723
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3674
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31661
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3374
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 828
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 637
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: CG
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD

11-124746368-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124746368
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124746368
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 1634
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.3G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2779+12G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.7G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.340+12G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2713+12G>A
  variant of: http://identifiers.org/hgnc/13433
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34718
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4556
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3299
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3613
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31322
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 923
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

11-124746395-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124746395
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124746395
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 588
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.340+39A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.14A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.30A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2779+39A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.34A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2713+39A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.14A>G
  variant of: http://identifiers.org/hgnc/13433
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3936
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34030
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1546
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 963
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7524
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1635
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

11-124746403-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124746403
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124746403
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 496
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.340+47G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.38G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.22G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.22G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.42G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2713+47G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2779+47G>A
  variant of: http://identifiers.org/hgnc/13433
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4064
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34347
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1167
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1394
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9816
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

11-124747010-TCTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747010
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747007
    reference: chr 11
allele count: 2
allele frequency: 1.656369569178275e-5
allele num: 120746
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.206-43_206-41delCTC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.463+186_463+188delCTC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.254-43_254-41delCTC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.59-149_59-147delCTC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.301_303delCTC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2714-43_2714-41delCTC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.112-43_112-41delCTC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.305_307delCTC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.88-43_88-41delCTC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.653_655delCTC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.108-43_108-41delCTC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.92-43_92-41delCTC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.235+186_235+188delCTC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.448-43_448-41delCTC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2780-43_2780-41delCTC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.341-43_341-41delCTC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.108-149_108-147delCTC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.92-167_92-165delCTC
  variant of: http://identifiers.org/hgnc/13433
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1855
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5423
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2457
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: TCTC
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum

11-124747014-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747014
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747014
    reference: chr 11
allele count: 1
allele frequency: 8.282122210995345e-6
allele num: 120742
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.206-43C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.301C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.254-43C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.108-149C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.112-43C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2714-43C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.88-43C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2780-43C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.653C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.92-167C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.448-43C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.108-43C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.305C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.463+186C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.59-149C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.341-43C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.235+186C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.92-43C>T
  variant of: http://identifiers.org/hgnc/13433
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6899
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2457
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6777
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6609
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

11-124747023-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747023
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747023
    reference: chr 11
allele count: 3
allele frequency: 2.484554353767412e-5
allele num: 120746
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.59-140C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.254-34C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.235+195C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.314C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.112-34C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.206-34C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.108-34C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.662C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.108-140C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.448-34C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.310C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.92-34C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2780-34C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2714-34C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.341-34C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.463+195C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.88-34C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.92-158C>T
  variant of: http://identifiers.org/hgnc/13433
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2458
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5422
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3033
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: African
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

11-124747024-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747024
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747024
    reference: chr 11
allele count: 2
allele frequency: 1.656369569178275e-5
allele num: 120746
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2714-33C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.254-33C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.88-33C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.92-157C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.311C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.315C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.663C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.112-33C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.59-139C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.235+196C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.108-139C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.448-33C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.92-33C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2780-33C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.341-33C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.206-33C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.108-33C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.463+196C>T
  variant of: http://identifiers.org/hgnc/13433
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2457
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5178
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6900
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4484
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum

11-124747031-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747031
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747031
    reference: chr 11
allele count: 1
allele frequency: 8.281847845891375e-6
allele num: 120746
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.92-26T>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.235+203T>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.92-150T>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.670T>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.448-26T>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.322T>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.112-26T>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.341-26T>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.108-132T>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.318T>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.463+203T>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.206-26T>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.59-132T>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2780-26T>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.88-26T>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2714-26T>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.254-26T>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.108-26T>G
  variant of: http://identifiers.org/hgnc/13433
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4484
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6900
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3389
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

11-124747034-T-TC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747034
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747035
    reference: chr 11
allele count: 1
allele frequency: 8.281985026171072e-6
allele num: 120744
alternate allele: TC
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.206-20dupC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.463+209dupC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.254-20dupC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.341-20dupC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.328dupC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.448-20dupC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.676dupC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2714-20dupC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.92-20dupC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.235+209dupC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.112-20dupC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.88-20dupC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.324dupC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.59-126dupC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.92-144dupC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2780-20dupC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.108-126dupC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.108-20dupC
  variant of: http://identifiers.org/hgnc/13433
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2457
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3033
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5176
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP

11-124747038-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747038
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747038
    reference: chr 11
allele count: 1
allele frequency: 8.281573498964803e-6
allele num: 120750
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.59-125A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.112-19A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.88-19A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.235+210A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.341-19A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.108-125A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.677A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.92-19A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2714-19A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.463+210A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.92-143A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.206-19A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.448-19A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.325A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.329A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.108-19A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2780-19A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.254-19A>G
  variant of: http://identifiers.org/hgnc/13433
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6779
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3033
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5423
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

11-124747044-T-TC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747044
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747045
    reference: chr 11
allele count: 1
allele frequency: 8.281162012653616e-6
allele num: 120756
alternate allele: TC
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.92-135dupC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.112-11dupC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.333dupC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.337dupC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.92-11dupC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.108-11dupC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.254-11dupC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.685dupC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2780-11dupC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.206-11dupC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2714-11dupC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.59-117dupC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.235+218dupC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.341-11dupC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.88-11dupC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.108-117dupC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.448-11dupC
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.463+218dupC
  variant of: http://identifiers.org/hgnc/13433
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4484
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6611
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5423
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-124747055-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747055
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747055
    reference: chr 11
allele count: 1
allele frequency: 8.280887711162637e-6
allele num: 120760
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.108-108A>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.448-2A>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.342A>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.235+227A>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2714-2A>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.254-2A>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.694A>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.463+227A>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.112-2A>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2780-2A>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.92-2A>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.206-2A>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.88-2A>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.108-2A>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.92-126A>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.59-108A>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.346A>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.341-2A>C
  variant of: http://identifiers.org/hgnc/13433
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5422
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2457
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6611
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6900
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4318
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2780-2A>C
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum

11-124747067-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747067
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747067
    reference: chr 11
allele count: 4
allele frequency: 3.312245371137094e-5
allele num: 120764
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.706C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2724C>T
  hgvsp: ENST00000538940.1:c.2724C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2790C>T
  hgvsp: ENST00000397801.1:c.2790C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.98C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.235+239C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.216C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.351C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.264C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.354C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.108-96C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.118C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.463+239C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.59-96C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.358C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.122C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.458C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.92-114C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.102C>T
  variant of: http://identifiers.org/hgnc/13433
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3035
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala930Ala
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

11-124747069-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747069
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747069
    reference: chr 11
allele count: 19
allele frequency: 1.57331655129012e-4
allele num: 120764
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.124A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.360A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.100A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.463+241A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.218A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.460A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.108-94A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.92-112A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2726A>G
  hgvsp: ENSP00000441797.1:p.Tyr909Cys
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2792A>G
  hgvsp: ENSP00000380903.1:p.Tyr931Cys
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.120A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.59-94A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.353A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.104A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.708A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.356A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.266A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.235+241A>G
  variant of: http://identifiers.org/hgnc/13433
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5844
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3035
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6779
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr931Cys
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS

http://identifiers.org/exac.variant/11-124747074-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747074
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747074
    reference: chr 11
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.59-89C>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.235+246C>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.713C>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.125C>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.109C>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2797C>A
  hgvsp: ENSP00000380903.1:p.Pro933Thr
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.129C>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.463+246C>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2731C>A
  hgvsp: ENSP00000441797.1:p.Pro911Thr
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.465C>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.223C>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.361C>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.105C>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.365C>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.358C>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.108-89C>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.271C>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.92-107C>A
  variant of: http://identifiers.org/hgnc/13433
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6611
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1734
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6781
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro933Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: VQSLOD

11-124747074-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747074
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747074
    reference: chr 11
allele count: 6
allele frequency: 4.968450340338848e-5
allele num: 120762
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.271C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.463+246C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.105C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.223C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.129C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.713C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.358C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.365C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.125C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.465C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2731C>G
  hgvsp: ENSP00000441797.1:p.Pro911Ala
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.59-89C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.235+246C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2797C>G
  hgvsp: ENSP00000380903.1:p.Pro933Ala
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.109C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.108-89C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.92-107C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.361C>G
  variant of: http://identifiers.org/hgnc/13433
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6902
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5423
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4486
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro933Ala
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

11-124747077-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747077
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747077
    reference: chr 11
allele count: 1
allele frequency: 8.280613427842734e-6
allele num: 120764
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.59-86G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.132G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2734G>C
  hgvsp: ENSP00000441797.1:p.Ala912Pro
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.112G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.92-104G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.361G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.716G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.235+249G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2800G>C
  hgvsp: ENSP00000380903.1:p.Ala934Pro
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.128G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.364G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.226G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.108-86G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.463+249G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.274G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.368G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.108G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.468G>C
  variant of: http://identifiers.org/hgnc/13433
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1734
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1859
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6611
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4485
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala934Pro
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

11-124747079-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747079
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747078
    reference: chr 11
allele count: 1
allele frequency: 8.280613427842734e-6
allele num: 120764
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.463+253delG
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.364+1delG
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.720delG
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.230delG
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.59-82delG
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.111+1delG
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2803+1delG
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.277+1delG
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.92-100delG
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.371+1delG
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.115+1delG
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.131+1delG
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2737+1delG
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.367+1delG
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.136delG
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.108-82delG
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.471+1delG
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.235+253delG
  variant of: http://identifiers.org/hgnc/13433
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4318
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: AG
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

11-124747080-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747080
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747080
    reference: chr 11
allele count: 2
allele frequency: 1.656150113446283e-5
allele num: 120762
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.463+252G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2737G>C
  hgvsp: ENSP00000441797.1:p.Val913Leu
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.367G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.364G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.371G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.277G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.92-101G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.229G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2803G>C
  hgvsp: ENSP00000380903.1:p.Val935Leu
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.719G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.108-83G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.471G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.131G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.135G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.111G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.59-83G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.115G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.235+252G>C
  variant of: http://identifiers.org/hgnc/13433
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6782
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5848
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val935Leu
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

11-124747082-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747082
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747082
    reference: chr 11
allele count: 12
allele frequency: 9.946619807035576e-5
allele num: 120644
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.277+2T>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.59-81T>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.131+2T>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.364+2T>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.92-99T>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.231T>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.111+2T>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.463+254T>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.367+2T>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.721T>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.471+2T>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.371+2T>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2737+2T>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.108-81T>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2803+2T>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.115+2T>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.137T>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.235+254T>G
  variant of: http://identifiers.org/hgnc/13433
canonical: true
consequence: splice donor
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3390
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6774
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1735
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.2803+2T>G
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

11-124747087-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747087
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747087
    reference: chr 11
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.364+7C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.726C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.131+7C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.108-76C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.92-94C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.59-76C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.471+7C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.277+7C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.367+7C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.236C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.115+7C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.371+7C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.111+7C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2803+7C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.235+259C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2737+7C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.463+259C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.142C>T
  variant of: http://identifiers.org/hgnc/13433
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5151
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2803+7C>T
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff

11-124747088-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747088
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747088
    reference: chr 11
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.471+8A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2803+8A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2737+8A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.59-75A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.131+8A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.237A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.364+8A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.371+8A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.727A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.115+8A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.108-75A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.235+260A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.367+8A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.463+260A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.143A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.111+8A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.277+8A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.92-93A>G
  variant of: http://identifiers.org/hgnc/13433
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6908
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5420
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2803+8A>G
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

11-124747093-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747093
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747093
    reference: chr 11
allele count: 2
allele frequency: 1.656150113446283e-5
allele num: 120762
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.235+265T>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.367+13T>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2803+13T>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.364+13T>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.242T>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.277+13T>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.371+13T>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.148T>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.732T>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.463+265T>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.471+13T>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.59-70T>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.131+13T>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.111+13T>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.92-88T>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.115+13T>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2737+13T>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.108-70T>C
  variant of: http://identifiers.org/hgnc/13433
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5420
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5151
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6599
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6909
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1860
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff

11-124747101-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747101
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747100
    reference: chr 11
allele count: 50
allele frequency: 4.140375283615707e-4
allele num: 120762
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.111+25delG
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.59-58delG
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.744delG
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.371+25delG
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.471+25delG
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2803+25delG
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.160delG
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.108-58delG
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.367+25delG
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.235+277delG
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.115+25delG
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.277+25delG
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.131+25delG
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.463+277delG
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.254delG
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.92-76delG
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.364+25delG
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2737+25delG
  variant of: http://identifiers.org/hgnc/13433
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2452
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4311
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5162
  bin: 9.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: TG
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff

11-124747103-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747103
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747103
    reference: chr 11
allele count: 1
allele frequency: 8.28775070445881e-6
allele num: 120660
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.131+23G>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2803+23G>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.252G>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.59-60G>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.111+23G>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.742G>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2737+23G>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.235+275G>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.158G>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.108-60G>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.371+23G>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.277+23G>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.364+23G>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.115+23G>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.471+23G>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.463+275G>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.367+23G>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.92-78G>T
  variant of: http://identifiers.org/hgnc/13433
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5157
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1725
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3036
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

http://identifiers.org/exac.variant/11-124747112-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747112
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747112
    reference: chr 11
allele count: 1
allele frequency: 8.281847845891375e-6
allele num: 120746
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.367+32C>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.108-51C>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.167C>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.751C>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2803+32C>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.235+284C>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.111+32C>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.131+32C>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.59-51C>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.364+32C>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.277+32C>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2737+32C>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.371+32C>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.115+32C>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.261C>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.463+284C>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.92-69C>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.471+32C>A
  variant of: http://identifiers.org/hgnc/13433
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5127
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5427
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-124747112-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747112
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747112
    reference: chr 11
allele count: 2
allele frequency: 1.656369569178275e-5
allele num: 120746
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.471+32C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.108-51C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.115+32C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.235+284C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.751C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.463+284C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.277+32C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.167C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.261C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.367+32C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2803+32C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.371+32C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.111+32C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.59-51C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2737+32C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.364+32C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.131+32C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.92-69C>T
  variant of: http://identifiers.org/hgnc/13433
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1860
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6778
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4312
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

11-124747117-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747117
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747117
    reference: chr 11
allele count: 83
allele frequency: 6.873933712089841e-4
allele num: 120746
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.108-46C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.172C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2803+37C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.115+37C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.266C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.364+37C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.59-46C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.92-64C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.756C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2737+37C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.367+37C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.235+289C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.277+37C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.471+37C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.131+37C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.463+289C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.371+37C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.111+37C>G
  variant of: http://identifiers.org/hgnc/13433
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3386
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5423
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1860
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6604
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ

11-124747118-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747118
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747118
    reference: chr 11
allele count: 1
allele frequency: 8.281710670156027e-6
allele num: 120748
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.277+38G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.463+290G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.371+38G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.59-45G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.235+290G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2737+38G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.173G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.108-45G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.757G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.367+38G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.92-63G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.471+38G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.131+38G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.111+38G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.267G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.115+38G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2803+38G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.364+38G>A
  variant of: http://identifiers.org/hgnc/13433
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3387
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3037
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4505
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4314
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

11-124747120-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747120
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747120
    reference: chr 11
allele count: 2
allele frequency: 1.656150113446283e-5
allele num: 120762
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2803+40G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.471+40G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.115+40G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.235+292G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.277+40G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.367+40G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.759G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.175G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2737+40G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.111+40G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.131+40G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.59-43G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.269G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.92-61G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.371+40G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.463+292G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.108-43G>C
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.364+40G>C
  variant of: http://identifiers.org/hgnc/13433
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6617
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4502
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP

11-124747127-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747127
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747127
    reference: chr 11
allele count: 6
allele frequency: 4.968532626697582e-5
allele num: 120760
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.182C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.115+47C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.132-36C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.278-36C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2804-36C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.472-36C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.236-288C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2738-36C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.276C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.766C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.367+47C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.365-36C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.59-36C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.372-36C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.92-54C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.112-36C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.108-36C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.464-288C>T
  variant of: http://identifiers.org/hgnc/13433
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6921
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5852
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3039
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff

11-124747134-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747134
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747134
    reference: chr 11
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.189T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.115+54T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.132-29T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.773T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.372-29T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2804-29T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.59-29T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.92-47T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.464-281T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.278-29T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.283T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.367+54T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.108-29T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.236-281T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.472-29T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.365-29T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.112-29T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2738-29T>A
  variant of: http://identifiers.org/hgnc/13433
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3039
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4501
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: African
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

11-124747135-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747135
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747135
    reference: chr 11
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.278-28C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.190C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.112-28C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.367+55C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.372-28C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.132-28C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.236-280C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.774C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.284C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.472-28C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.59-28C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.115+55C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.108-28C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2738-28C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2804-28C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.365-28C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.464-280C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.92-46C>T
  variant of: http://identifiers.org/hgnc/13433
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4501
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5074
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-124747147-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747147
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747147
    reference: chr 11
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.786C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.236-268C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.202C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.59-16C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.296C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.112-16C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.278-16C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.372-16C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.132-16C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.108-16C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.115+67C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2738-16C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2804-16C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.365-16C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.367+67C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.92-34C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.472-16C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.464-268C>T
  variant of: http://identifiers.org/hgnc/13433
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3041
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4314
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

11-124747150-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747150
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747150
    reference: chr 11
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.789T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.372-13T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.278-13T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.464-265T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.59-13T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.115+70T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.299T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.236-265T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2804-13T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.92-31T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.365-13T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.132-13T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.367+70T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.108-13T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.472-13T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.205T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2738-13T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.112-13T>A
  variant of: http://identifiers.org/hgnc/13433
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3040
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6788
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6618
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

11-124747152-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747152
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747152
    reference: chr 11
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.472-11A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.207A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.372-11A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.367+72A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.236-263A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.132-11A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.301A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.791A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.278-11A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.115+72A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.59-11A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.365-11A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2804-11A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.108-11A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.92-29A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.112-11A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.464-263A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2738-11A>G
  variant of: http://identifiers.org/hgnc/13433
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5071
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3040
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

11-124747170-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747170
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747170
    reference: chr 11
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.115C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.479C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.236-245C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.464-245C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.139C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.379C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.809C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.66C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2745C>T
  hgvsp: ENST00000538940.1:c.2745C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.225C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.119C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.92-11C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2811C>T
  hgvsp: ENST00000397801.1:c.2811C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.372C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.285C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.115+90C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.319C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.367+90C>T
  variant of: http://identifiers.org/hgnc/13433
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5433
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5070
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5853
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe937Phe
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

11-124747183-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747183
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747183
    reference: chr 11
allele count: 1
allele frequency: 8.280887711162637e-6
allele num: 120760
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.385G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.238G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.94G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.132G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.492G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.392G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.298G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.79G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2758G>A
  hgvsp: ENSP00000441797.1:p.Gly920Ser
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.332G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.822G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.464-232G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.128G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2824G>A
  hgvsp: ENSP00000380903.1:p.Gly942Ser
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.236-232G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.367+103G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.152G>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.115+103G>A
  variant of: http://identifiers.org/hgnc/13433
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3041
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4502
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5853
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6924
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly942Ser
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ

11-124747189-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747189
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747189
    reference: chr 11
allele count: 1
allele frequency: 8.280887711162637e-6
allele num: 120760
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.85T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2764T>A
  hgvsp: ENSP00000441797.1:p.Ser922Thr
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.398T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.498T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.304T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2830T>A
  hgvsp: ENSP00000380903.1:p.Ser944Thr
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.367+109T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.100T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.138T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.158T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.828T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.391T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.244T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.338T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.115+109T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.134T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.236-226T>A
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.464-226T>A
  variant of: http://identifiers.org/hgnc/13433
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4502
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser944Thr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
reference allele: T
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

11-124747197-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747197
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747197
    reference: chr 11
allele count: 1
allele frequency: 8.280887711162637e-6
allele num: 120760
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.236-218C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.464-218C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.252C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.93C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.142C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.406C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.836C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.108C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.312C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.399C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2838C>T
  hgvsp: ENST00000397801.1:c.2838C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.166C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.367+117C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2772C>T
  hgvsp: ENST00000538940.1:c.2772C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.115+117C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.146C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.506C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.346C>T
  variant of: http://identifiers.org/hgnc/13433
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1725
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4502
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala946Ala
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ

11-124747202-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747202
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747202
    reference: chr 11
allele count: 1
allele frequency: 8.281024859636628e-6
allele num: 120758
alternate allele: T
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.367+122C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.98C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.151C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.317C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.511C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.464-213C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.236-213C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2843C>T
  hgvsp: ENSP00000380903.1:p.Ser948Phe
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.841C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.113C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.257C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2777C>T
  hgvsp: ENSP00000441797.1:p.Ser926Phe
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.404C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.411C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.115+122C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.351C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.171C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.147C>T
  variant of: http://identifiers.org/hgnc/13433
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser948Phe
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum

11-124747214-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747214
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747214
    reference: chr 11
allele count: 1
allele frequency: 8.281162012653616e-6
allele num: 120756
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.260+9C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.101+9C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.514+9C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.174+9C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.320+9C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.367+134C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.853C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.150+9C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.115+134C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.407+9C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.464-201C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.363C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2780+9C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.414+9C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2846+9C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.236-201C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.154+9C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.116+9C>T
  variant of: http://identifiers.org/hgnc/13433
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1726
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3041
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6922
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4316
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

11-124747214-CTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747214
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747212
    reference: chr 11
allele count: 1
allele frequency: 8.281162012653616e-6
allele num: 120756
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.150+10_150+11delTT
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.367+135_367+136delTT
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.260+10_260+11delTT
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.236-200_236-199delTT
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.414+10_414+11delTT
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.364_365delTT
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.854_855delTT
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.407+10_407+11delTT
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.464-200_464-199delTT
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.101+10_101+11delTT
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2846+10_2846+11delTT
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2780+10_2780+11delTT
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.320+10_320+11delTT
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.116+10_116+11delTT
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.174+10_174+11delTT
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.154+10_154+11delTT
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.115+135_115+136delTT
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.514+10_514+11delTT
  variant of: http://identifiers.org/hgnc/13433
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4502
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6617
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: African
reference allele: CTT
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum

11-124747219-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747219
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747219
    reference: chr 11
allele count: 1
allele frequency: 8.281299170213822e-6
allele num: 120754
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.514+14C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.115+139C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2846+14C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2780+14C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.858C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.464-196C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.367+139C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.101+14C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.407+14C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.320+14C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.236-196C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.368C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.150+14C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.116+14C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.414+14C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.174+14C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.260+14C>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.154+14C>G
  variant of: http://identifiers.org/hgnc/13433
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6788
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6922
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

11-124747220-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747220
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747220
    reference: chr 11
allele count: 1
allele frequency: 8.281436332317477e-6
allele num: 120752
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.260+15C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.369C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.174+15C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.150+15C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.414+15C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.236-195C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2846+15C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.320+15C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.367+140C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.514+15C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.407+15C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.464-195C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.859C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.115+140C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2780+15C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.101+15C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.154+15C>T
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.116+15C>T
  variant of: http://identifiers.org/hgnc/13433
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 5432
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5854
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6789
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

11-124747222-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 124747222
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 124747222
    reference: chr 11
allele count: 2
allele frequency: 1.656287266463495e-5
allele num: 120752
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000380903
  ensembl transcript: ENST00000397801
  gene symbol: ROBO3
  hgvsc: ENST00000397801.1:c.2846+17A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531075
  gene symbol: ROBO3
  hgvsc: ENST00000531075.1:n.101+17A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000529658
  gene symbol: ROBO3
  hgvsc: ENST00000529658.1:n.464-193A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000532472
  gene symbol: ROBO3
  hgvsc: ENST00000532472.1:n.367+142A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531119
  gene symbol: ROBO3
  hgvsc: ENST00000531119.1:n.260+17A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525482
  gene symbol: ROBO3
  hgvsc: ENST00000525482.1:n.115+142A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527245
  gene symbol: ROBO3
  hgvsc: ENST00000527245.1:n.861A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528144
  gene symbol: ROBO3
  hgvsc: ENST00000528144.1:n.236-193A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000526551
  gene symbol: ROBO3
  hgvsc: ENST00000526551.1:n.174+17A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531888
  gene symbol: ROBO3
  hgvsc: ENST00000531888.1:n.371A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000531545
  gene symbol: ROBO3
  hgvsc: ENST00000531545.1:n.320+17A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000530647
  gene symbol: ROBO3
  hgvsc: ENST00000530647.1:n.150+17A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528068
  gene symbol: ROBO3
  hgvsc: ENST00000528068.1:n.414+17A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000534598
  gene symbol: ROBO3
  hgvsc: ENST00000534598.1:n.154+17A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl protein: ENSP00000441797
  ensembl transcript: ENST00000538940
  gene symbol: ROBO3
  hgvsc: ENST00000538940.1:c.2780+17A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000525448
  gene symbol: ROBO3
  hgvsc: ENST00000525448.1:n.514+17A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000527196
  gene symbol: ROBO3
  hgvsc: ENST00000527196.1:n.407+17A>G
  variant of: http://identifiers.org/hgnc/13433
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154134
  ensembl transcript: ENST00000528820
  gene symbol: ROBO3
  hgvsc: ENST00000528820.1:n.116+17A>G
  variant of: http://identifiers.org/hgnc/13433
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4315
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5066
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6617
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: A

GenotypeQuality
all individuals: 34309
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1155
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5273
bin: 9.75e1
variant carriers: 1

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

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

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

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

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.941e1

FS
type: SiteQuality
SIO_000300: 8.818e0

DP
type: SiteQuality
SIO_000300: 1.688205e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.33e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.886e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.17e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -5.052e0

QD
type: SiteQuality
SIO_000300: 1.118e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.78e-1

GenotypeQuality
all individuals: 2
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1954
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1276
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 144
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 68
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.645e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.57e-2

DP
type: SiteQuality
SIO_000300: 1.63864e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.2e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.2e-1

QD
type: SiteQuality
SIO_000300: 3.073e1

GenotypeQuality
all individuals: 2
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 154
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 74
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 126
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 2.384737678855326e-3
allele num: 1258
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2062
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

DP
type: SiteQuality
SIO_000300: 1.63858e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.51e-2

FS
type: SiteQuality
SIO_000300: 9.882e0

QD
type: SiteQuality
SIO_000300: 1.25e1

VQSLOD
type: SiteQuality
SIO_000300: -2.592e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 114
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1160
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2102
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 140
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 170
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 68
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.64e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.48e-1

QD
type: SiteQuality
SIO_000300: 6.96e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.61085e5

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 116
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1022
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 98
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 152
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2178
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.517e0

DP
type: SiteQuality
SIO_000300: 1.59007e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.517e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.164e0

QD
type: SiteQuality
SIO_000300: 9.56e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.840000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.690000000000001e-2

GenotypeQuality
all individuals: 32
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2182
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 152
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 100
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 116
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 9.727626459143969e-4
allele num: 1028
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.60228e5

BaseQRankSum
type: SiteQuality
SIO_000300: -2.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.77e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.184e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.76e-1

QD
type: SiteQuality
SIO_000300: 7.81e0

VQSLOD
type: SiteQuality
SIO_000300: -2.688e0

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 42
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 102
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 120
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1094
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 144
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2332
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.42e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.548e1

DP
type: SiteQuality
SIO_000300: 1.60717e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.63e-2

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1062
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 120
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2360
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 136
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 100
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.38e0

MQRankSum
type: SiteQuality
SIO_000300: -7.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.61e-2

DP
type: SiteQuality
SIO_000300: 1.60327e5

VQSLOD
type: SiteQuality
SIO_000300: -1.678e0

QD
type: SiteQuality
SIO_000300: 1.447e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 5275
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1069
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1155
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

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

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

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.34e-2

FS
type: SiteQuality
SIO_000300: 6.12e-1

DP
type: SiteQuality
SIO_000300: 1.68838e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.79e0

VQSLOD
type: SiteQuality
SIO_000300: 6.889999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.27e-1

QD
type: SiteQuality
SIO_000300: 1.367e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.091e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

GenotypeQuality
all individuals: 34258
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1077
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2709
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 3.501e0

QD
type: SiteQuality
SIO_000300: 1.776e1

MQRankSum
type: SiteQuality
SIO_000300: 4.35e-1

MQ
type: SiteQuality
SIO_000300: 5.446e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.76e0

DP
type: SiteQuality
SIO_000300: 1.689159e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.828e0

VQSLOD
type: SiteQuality
SIO_000300: -1.301e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.02e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.38e0

GenotypeQuality
all individuals: 4044
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8388
bin: 6.75e1
variant carriers: 0

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

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

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

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -4.432e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.52e0

FS
type: SiteQuality
SIO_000300: 1.054e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

MQRankSum
type: SiteQuality
SIO_000300: 3.18e-1

DP
type: SiteQuality
SIO_000300: 1.689355e6

QD
type: SiteQuality
SIO_000300: 1.365e1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 130
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.258389261744966e-3
allele num: 2384
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 120
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 98
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1048
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.60422e5

ClippingRankSum
type: SiteQuality
SIO_000300: -6.840000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.9e-3

FS
type: SiteQuality
SIO_000300: 2.039e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.599999999999999e-2

QD
type: SiteQuality
SIO_000300: 1.028e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.45e-1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

Other
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allele frequency: 0.0e0
allele num: 40
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
allele num: 116
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 1002
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 2444
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.6076e5

InbreedingCoeff
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SIO_000300: -8.71e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.5e-1

FS
type: SiteQuality
SIO_000300: 4.593e0

ReadPosRankSum
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SIO_000300: 5.5e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.547e0

QD
type: SiteQuality
SIO_000300: 8.41e0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 116
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 20
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 46
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 68
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 2934
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 116
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1028
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
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SIO_000300: -1.746e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

QD
type: SiteQuality
SIO_000300: 1.148e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.87e-2

MQRankSum
type: SiteQuality
SIO_000300: -9.22e-1

DP
type: SiteQuality
SIO_000300: 1.63019e5

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 110
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South Asian
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allele frequency: 0.0e0
allele num: 2628
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 94
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.51e-1

DP
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SIO_000300: 1.51803e5

MQRankSum
type: SiteQuality
SIO_000300: -7.51e-1

QD
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SIO_000300: 1.425e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.51e-1

InbreedingCoeff
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SIO_000300: -9.089999999999999e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.674e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.51e-1

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 90
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 106
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

South Asian
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allele frequency: 4.035512510088781e-4
allele num: 2478
num of homozygotes: 0

Other
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allele num: 34
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ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 8.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: 6.759999999999999e-2

DP
type: SiteQuality
SIO_000300: 1.47943e5

VQSLOD
type: SiteQuality
SIO_000300: 2.9e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.59e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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bin: 7.25e1
variant carriers: 1

East Asian
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allele frequency: 0.0e0
allele num: 90
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 2478
num of homozygotes: 0

Latino
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allele frequency: 2.777777777777778e-2
allele num: 36
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.9e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.759999999999999e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.59e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

FS
type: SiteQuality
SIO_000300: 8.31e-1

QD
type: SiteQuality
SIO_000300: 1.282e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.47943e5

GenotypeQuality
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 106
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 766
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 78
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 32
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 2242
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.262e1

MQRankSum
type: SiteQuality
SIO_000300: -1.98e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.98e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.27e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.41804e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

Latino
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allele frequency: 0.0e0
allele num: 16
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 458
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 86
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 44
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 16
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1300
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.222e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.63e-2

DP
type: SiteQuality
SIO_000300: 1.24774e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.98e0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 42
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 16
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 1236
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 430
num of homozygotes: 0

Other
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allele num: 12
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

QD
type: SiteQuality
SIO_000300: 8.94e0

FS
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SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -9.669999999999999e-2

MQ
type: SiteQuality
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DP
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SIO_000300: 1.24265e5

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

VQSLOD
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GenotypeQuality
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bin: 1.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele frequency: 0.0e0
allele num: 1080
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African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 386
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.679e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

ClippingRankSum
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SIO_000300: 7.36e-1

VQSLOD
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MQ
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InbreedingCoeff
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QD
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MQRankSum
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DP
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ReadPosRankSum
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GenotypeQuality
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variant carriers: 0

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

Latino
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allele frequency: 0.0e0
allele num: 8
num of homozygotes: 0

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

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

South Asian
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allele frequency: 0.0e0
allele num: 340
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 148
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
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DP
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InbreedingCoeff
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SIO_000300: -1.06e-1

VQSLOD
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FS
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ClippingRankSum
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ReadPosRankSum
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QD
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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Other
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European (Finnish)
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East Asian
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

MQRankSum
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SIO_000300: 9.3e-1

MQ
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SIO_000300: 5.982e1

BaseQRankSum
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SIO_000300: -8.28e-1

VQSLOD
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QD
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SIO_000300: 1.468e1

ClippingRankSum
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SIO_000300: -1.872e0

InbreedingCoeff
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SIO_000300: 4.4e-3

ReadPosRankSum
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SIO_000300: -1.341e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.028589e6

GenotypeDepth
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variant carriers: 0

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

African
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allele frequency: 1.02082482645978e-4
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num of homozygotes: 0

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

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

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

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

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

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

BaseQRankSum
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SIO_000300: 2.38e-1

MQRankSum
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QD
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InbreedingCoeff
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FS
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SIO_000300: 5.85e-1

VQSLOD
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SIO_000300: 8.8e-1

ClippingRankSum
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SIO_000300: 9.82e-1

ReadPosRankSum
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SIO_000300: 2.53e-1

MQ
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SIO_000300: 6.0e1

DP
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GenotypeDepth
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 1
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allele num: 66736
num of homozygotes: 0

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

African
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allele count: 0
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num of homozygotes: 0

Other
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.01e0

MQRankSum
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SIO_000300: 5.39e-1

VQSLOD
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FS
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SIO_000300: 5.237e0

ClippingRankSum
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SIO_000300: -5.76e-1

MQ
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SIO_000300: 5.999e1

QD
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SIO_000300: 1.066e1

DP
type: SiteQuality
SIO_000300: 4.028868e6

InbreedingCoeff
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SIO_000300: 2.3e-3

ReadPosRankSum
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SIO_000300: 1.94e-1

GenotypeDepth
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 1
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allele num: 66738
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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num of homozygotes: 0

ReadPosRankSum
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SIO_000300: 5.11e-1

InbreedingCoeff
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BaseQRankSum
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VQSLOD
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MQ
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ClippingRankSum
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DP
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QD
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FS
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MQRankSum
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SIO_000300: -9.72e-1

GenotypeDepth
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variant carriers: 0

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

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

European (Non-Finnish)
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allele frequency: 5.993586862057598e-5
allele num: 66738
num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 2.846953759477359e-4
allele num: 66738
num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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East Asian
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South Asian
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MQ
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ClippingRankSum
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BaseQRankSum
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FS
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ReadPosRankSum
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DP
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QD
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MQRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Non-Finnish)
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South Asian
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European (Finnish)
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African
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East Asian
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ReadPosRankSum
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ClippingRankSum
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FS
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VQSLOD
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QD
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BaseQRankSum
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MQRankSum
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MQ
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InbreedingCoeff
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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Latino
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African
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Other
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European (Non-Finnish)
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MQRankSum
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QD
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MQ
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ReadPosRankSum
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FS
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VQSLOD
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DP
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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African
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European (Finnish)
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South Asian
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European (Non-Finnish)
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InbreedingCoeff
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MQ
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DP
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ClippingRankSum
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FS
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QD
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VQSLOD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Other
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European (Finnish)
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African
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Latino
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European (Non-Finnish)
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East Asian
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QD
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VQSLOD
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DP
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MQ
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InbreedingCoeff
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MQRankSum
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FS
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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South Asian
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European (Non-Finnish)
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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FS
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MQ
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DP
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MQRankSum
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QD
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Finnish)
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South Asian
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European (Non-Finnish)
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Latino
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Other
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VQSLOD
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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MQ
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QD
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FS
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BaseQRankSum
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DP
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InbreedingCoeff
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SIO_000300: 8.800000000000001e-3

GenotypeDepth
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variant carriers: 0

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

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

African
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Latino
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South Asian
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European (Non-Finnish)
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European (Finnish)
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num of homozygotes: 0

Other
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InbreedingCoeff
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MQ
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QD
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ReadPosRankSum
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DP
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VQSLOD
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MQRankSum
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FS
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SIO_000300: 8.56e-1

BaseQRankSum
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ClippingRankSum
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GenotypeDepth
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variant carriers: 0

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

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

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

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

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

Other
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FS
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QD
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MQRankSum
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InbreedingCoeff
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MQ
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DP
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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SIO_000300: -4.1e-2

GenotypeDepth
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variant carriers: 0

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

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

East Asian
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Latino
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
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African
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Other
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South Asian
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VQSLOD
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MQ
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FS
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BaseQRankSum
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QD
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ClippingRankSum
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MQRankSum
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DP
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InbreedingCoeff
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SIO_000300: 4.1e-3

ReadPosRankSum
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele num: 9798
num of homozygotes: 0

East Asian
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European (Non-Finnish)
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allele count: 74
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allele num: 66722
num of homozygotes: 0

Other
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European (Finnish)
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allele count: 1
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allele num: 6614
num of homozygotes: 0

Latino
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allele count: 3
allele frequency: 2.591568762957844e-4
allele num: 11576
num of homozygotes: 0

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

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

South Asian
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allele num: 16512
num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

Other
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East Asian
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allele count: 2
allele frequency: 2.318571759795966e-4
allele num: 8626
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
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InbreedingCoeff
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QD
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MQRankSum
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ClippingRankSum
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FS
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ReadPosRankSum
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MQ
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VQSLOD
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DP
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GenotypeDepth
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variant carriers: 0

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

African
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allele count: 0
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East Asian
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DP
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ReadPosRankSum
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QD
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BaseQRankSum
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VQSLOD
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MQRankSum
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MQ
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FS
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ClippingRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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African
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European (Finnish)
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MQ
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FS
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BaseQRankSum
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QD
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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MQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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European (Finnish)
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African
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South Asian
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Latino
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MQRankSum
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VQSLOD
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BaseQRankSum
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FS
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InbreedingCoeff
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QD
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DP
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MQ
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ReadPosRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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Other
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European (Non-Finnish)
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African
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European (Finnish)
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South Asian
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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DP
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MQRankSum
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MQ
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FS
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QD
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BaseQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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South Asian
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East Asian
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FS
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InbreedingCoeff
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MQ
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DP
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MQRankSum
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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QD
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East Asian
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European (Finnish)
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MQ
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FS
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ReadPosRankSum
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QD
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MQRankSum
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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DP
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African
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VQSLOD
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East Asian
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DP
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VQSLOD
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VQSLOD
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

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

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

InbreedingCoeff
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SIO_000300: 2.5e-3

VQSLOD
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SIO_000300: 2.53e0

FS
type: SiteQuality
SIO_000300: 6.67e-1

ClippingRankSum
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SIO_000300: 2.18e0

DP
type: SiteQuality
SIO_000300: 4.018955e6

MQ
type: SiteQuality
SIO_000300: 5.98e1

QD
type: SiteQuality
SIO_000300: 1.307e1

MQRankSum
type: SiteQuality
SIO_000300: -1.19e-1

BaseQRankSum
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SIO_000300: 3.98e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.01e-1

GenotypeDepth
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bin: 7.75e1
variant carriers: 1

GenotypeDepth
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bin: 7.5e0
variant carriers: 0

GenotypeDepth
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bin: 5.25e1
variant carriers: 0

GenotypeDepth
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bin: 2.75e1
variant carriers: 0

GenotypeDepth
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bin: 3.75e1
variant carriers: 0

GenotypeDepth
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bin: 9.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

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

South Asian
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allele num: 16512
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 4.018955e6

ReadPosRankSum
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SIO_000300: 8.01e-1

InbreedingCoeff
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SIO_000300: 2.5e-3

QD
type: SiteQuality
SIO_000300: 1.307e1

MQ
type: SiteQuality
SIO_000300: 5.98e1

MQRankSum
type: SiteQuality
SIO_000300: -1.19e-1

VQSLOD
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SIO_000300: 2.53e0

ClippingRankSum
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SIO_000300: 2.18e0

FS
type: SiteQuality
SIO_000300: 6.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.98e0

GenotypeDepth
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bin: 8.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 80
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 1
allele frequency: 1.159285879897983e-4
allele num: 8626
num of homozygotes: 0

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

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 7.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

FS
type: SiteQuality
SIO_000300: 6.412e0

MQRankSum
type: SiteQuality
SIO_000300: 2.26e-1

MQ
type: SiteQuality
SIO_000300: 5.983e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.610000000000001e-1

DP
type: SiteQuality
SIO_000300: 4.018764e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.29e-1

QD
type: SiteQuality
SIO_000300: 1.096e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.74e-1

VQSLOD
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QD
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DP
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ClippingRankSum
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MQRankSum
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FS
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SIO_000300: 3.6627e1

MQ
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SIO_000300: 5.858e1

InbreedingCoeff
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SIO_000300: 2.4e-3

BaseQRankSum
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GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

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

South Asian
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allele count: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 1

Other
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allele frequency: 0.0e0
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