15-38787015-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38787015
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38787015
    reference: chr 15
allele count: 2
allele frequency: 2.343347237193607e-5
allele num: 85348
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1730-47C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.2027-47C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1916-47C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.*105-47C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1874-47C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1768+3980C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1616-4126C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1769-47C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*178-47C>T
  variant of: http://identifiers.org/hgnc/9878
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2513
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2972
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17611
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8781
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10348
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12675
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3331
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1987
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12135
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

15-38787017-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38787017
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38787017
    reference: chr 15
allele count: 3
allele frequency: 3.557199772339215e-5
allele num: 84336
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1616-4128C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1768+3978C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1769-49C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.2027-49C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*178-49C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.*105-49C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1730-49C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1916-49C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1874-49C>T
  variant of: http://identifiers.org/hgnc/9878
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2987
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10453
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8688
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17529
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12649
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2589
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6199
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5093
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 813
  bin: 9.75e1
  variant carriers: 3
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

15-38790947-C-CCCTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38790947
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38790951
    reference: chr 15
allele count: 1
allele frequency: 8.575152637716951e-6
allele num: 116616
alternate allele: CCCTT
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*177+44_*177+47dupAAGG
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1768+44_1768+47dupAAGG
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1873+44_1873+47dupAAGG
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1768+44_1768+47dupAAGG
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1915+44_1915+47dupAAGG
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.2026+44_2026+47dupAAGG
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1729+44_1729+47dupAAGG
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1353_1615+1356dupAAGG
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.*104+44_*104+47dupAAGG
  variant of: http://identifiers.org/hgnc/9878
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2815
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3833
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1723
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3525
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10896
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23267
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10919
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6415
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1525
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1686
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ

15-38790951-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38790951
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38790951
    reference: chr 15
allele count: 1
allele frequency: 8.556076525548445e-6
allele num: 116876
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.*104+44A>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1729+44A>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*177+44A>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1768+44A>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1873+44A>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.2026+44A>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1915+44A>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1353A>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1768+44A>G
  variant of: http://identifiers.org/hgnc/9878
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11970
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3492
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10930
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2665
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2799
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23452
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37359
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1473
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1603
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: T
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

15-38790955-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38790955
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38790955
    reference: chr 15
allele count: 1
allele frequency: 8.550224015869215e-6
allele num: 116956
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*177+40T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1768+40T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1729+40T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1915+40T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.*104+40T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1873+40T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1768+40T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.2026+40T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1349T>C
  variant of: http://identifiers.org/hgnc/9878
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10988
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23687
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2798
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13181
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3143
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1203
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2694
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum

15-38790958-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38790958
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38790958
    reference: chr 15
allele count: 1
allele frequency: 8.536793580331227e-6
allele num: 117140
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1768+37A>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1729+37A>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.2026+37A>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*177+37A>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1346A>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.*104+37A>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1873+37A>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1915+37A>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1768+37A>T
  variant of: http://identifiers.org/hgnc/9878
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1651
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2771
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13966
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2801
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23797
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11031
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1657
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1201
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 732
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

15-38790959-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38790959
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38790959
    reference: chr 15
allele count: 1
allele frequency: 8.540438978563499e-6
allele num: 117090
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1729+36G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.2026+36G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1915+36G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*177+36G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1768+36G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1768+36G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1873+36G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.*104+36G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1345G>A
  variant of: http://identifiers.org/hgnc/9878
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2802
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11063
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14172
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2622
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23868
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2693
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 900
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1139
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD

15-38790966-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38790966
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38790966
    reference: chr 15
allele count: 1
allele frequency: 8.507452528414892e-6
allele num: 117544
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1729+29G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.2026+29G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1768+29G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1338G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1873+29G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1768+29G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*177+29G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.*104+29G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1915+29G>A
  variant of: http://identifiers.org/hgnc/9878
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15231
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1458
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24157
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11131
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2809
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1521
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1656
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

15-38790968-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38790968
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38790968
    reference: chr 15
allele count: 2
allele frequency: 1.698110003566031e-5
allele num: 117778
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1915+27T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1873+27T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1336T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*177+27T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.*104+27T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1768+27T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.2026+27T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1729+27T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1768+27T>C
  variant of: http://identifiers.org/hgnc/9878
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2805
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15549
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24222
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11153
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2695
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 703
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1655
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1448
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum

15-38790972-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38790972
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38790972
    reference: chr 15
allele count: 2
allele frequency: 1.693279374163943e-5
allele num: 118114
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1729+23C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1768+23C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.2026+23C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1768+23C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.*104+23C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1332C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1915+23C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1873+23C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*177+23C>T
  variant of: http://identifiers.org/hgnc/9878
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15949
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2808
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1242
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24350
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11196
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1665
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2692
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

15-38790976-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38790976
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38790976
    reference: chr 15
allele count: 2
allele frequency: 1.688077111362447e-5
allele num: 118478
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.*104+19C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1768+19C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*177+19C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.2026+19C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1915+19C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1873+19C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1328C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1768+19C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1729+19C>T
  variant of: http://identifiers.org/hgnc/9878
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16331
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24437
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11199
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2808
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1168
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43022
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 684
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

15-38790980-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38790980
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38790980
    reference: chr 15
allele count: 1
allele frequency: 8.414391976035812e-6
allele num: 118844
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1324G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.2026+15G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.*104+15G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1873+15G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1768+15G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*177+15G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1729+15G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1915+15G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1768+15G>A
  variant of: http://identifiers.org/hgnc/9878
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24609
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11248
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16609
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2803
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1688
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 955
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1470
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

15-38790983-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38790983
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38790983
    reference: chr 15
allele count: 1
allele frequency: 8.391514500537057e-6
allele num: 119168
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1915+12C>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1729+12C>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1321C>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1768+12C>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*177+12C>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1768+12C>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.*104+12C>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1873+12C>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.2026+12C>A
  variant of: http://identifiers.org/hgnc/9878
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2802
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11262
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24725
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16844
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 812
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2690
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: DP

15-38791004-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791004
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791004
    reference: chr 15
allele count: 1
allele frequency: 8.30813199960121e-6
allele num: 120364
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1300C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1864C>G
  hgvsp: ENSP00000310244.5:p.Leu622Val
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*168C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.*95C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1759C>G
  hgvsp: ENSP00000388540.2:p.Leu587Val
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1906C>G
  hgvsp: ENSP00000453583.1:p.Leu636Val
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.2017C>G
  hgvsp: ENSP00000452859.1:p.Leu673Val
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1720C>G
  hgvsp: ENSP00000444762.1:p.Leu574Val
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1759C>G
  hgvsp: ENSP00000452721.1:p.Leu587Val
  variant of: http://identifiers.org/hgnc/9878
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2812
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11406
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17335
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25289
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1139
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu622Val
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD

15-38791010-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791010
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791010
    reference: chr 15
allele count: 1
allele frequency: 8.300546175938376e-6
allele num: 120474
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1753A>G
  hgvsp: ENSP00000452721.1:p.Lys585Glu
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.*89A>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1294A>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1858A>G
  hgvsp: ENSP00000310244.5:p.Lys620Glu
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1900A>G
  hgvsp: ENSP00000453583.1:p.Lys634Glu
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.2011A>G
  hgvsp: ENSP00000452859.1:p.Lys671Glu
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1714A>G
  hgvsp: ENSP00000444762.1:p.Lys572Glu
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*162A>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1753A>G
  hgvsp: ENSP00000388540.2:p.Lys585Glu
  variant of: http://identifiers.org/hgnc/9878
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17371
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25337
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11418
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2815
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1141
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2695
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Lys620Glu
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum

15-38791019-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791019
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791019
    reference: chr 15
allele count: 9
allele frequency: 7.461201750895344e-5
allele num: 120624
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1705T>C
  hgvsp: ENST00000539159.1:c.1705T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1891T>C
  hgvsp: ENST00000558432.1:c.1891T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1744T>C
  hgvsp: ENST00000559830.1:c.1744T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.2002T>C
  hgvsp: ENST00000561180.1:c.2002T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*153T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1744T>C
  hgvsp: ENST00000450598.2:c.1744T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1849T>C
  hgvsp: ENST00000310803.5:c.1849T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.*80T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1285T>C
  variant of: http://identifiers.org/hgnc/9878
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11447
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17343
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2816
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25444
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44948
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1536
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu617Leu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

15-38791023-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791023
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791023
    reference: chr 15
allele count: 2
allele frequency: 1.657522666622466e-5
allele num: 120662
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1998C>T
  hgvsp: ENST00000561180.1:c.1998C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1281C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1701C>T
  hgvsp: ENST00000539159.1:c.1701C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1740C>T
  hgvsp: ENST00000450598.2:c.1740C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1740C>T
  hgvsp: ENST00000559830.1:c.1740C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.*76C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1845C>T
  hgvsp: ENST00000310803.5:c.1845C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1887C>T
  hgvsp: ENST00000558432.1:c.1887C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*149C>T
  variant of: http://identifiers.org/hgnc/9878
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17339
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2819
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11460
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6967
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Cys615Cys
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

15-38791032-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791032
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791032
    reference: chr 15
allele count: 1
allele frequency: 8.285690612312537e-6
allele num: 120690
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1692C>A
  hgvsp: ENST00000539159.1:c.1692C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1731C>A
  hgvsp: ENST00000559830.1:c.1731C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*140C>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1878C>A
  hgvsp: ENST00000558432.1:c.1878C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.*67C>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1836C>A
  hgvsp: ENST00000310803.5:c.1836C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1731C>A
  hgvsp: ENST00000450598.2:c.1731C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1989C>A
  hgvsp: ENST00000561180.1:c.1989C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1272C>A
  variant of: http://identifiers.org/hgnc/9878
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11475
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17324
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2817
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25499
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2694
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1541
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ser612Ser
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP

15-38791034-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791034
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791034
    reference: chr 15
allele count: 2
allele frequency: 1.657000828500414e-5
allele num: 120700
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1876T>A
  hgvsp: ENSP00000453583.1:p.Ser626Thr
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1834T>A
  hgvsp: ENSP00000310244.5:p.Ser612Thr
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1690T>A
  hgvsp: ENSP00000444762.1:p.Ser564Thr
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1987T>A
  hgvsp: ENSP00000452859.1:p.Ser663Thr
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.*65T>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*138T>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1270T>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1729T>A
  hgvsp: ENSP00000388540.2:p.Ser577Thr
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1729T>A
  hgvsp: ENSP00000452721.1:p.Ser577Thr
  variant of: http://identifiers.org/hgnc/9878
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17322
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2816
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11474
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25506
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2696
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Ser612Thr
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

15-38791037-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791037
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791037
    reference: chr 15
allele count: 1
allele frequency: 8.284592315212168e-6
allele num: 120706
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1831G>A
  hgvsp: ENSP00000310244.5:p.Val611Met
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1873G>A
  hgvsp: ENSP00000453583.1:p.Val625Met
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*135G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1726G>A
  hgvsp: ENSP00000452721.1:p.Val576Met
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1267G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.*62G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1687G>A
  hgvsp: ENSP00000444762.1:p.Val563Met
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1726G>A
  hgvsp: ENSP00000388540.2:p.Val576Met
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1984G>A
  hgvsp: ENSP00000452859.1:p.Val662Met
  variant of: http://identifiers.org/hgnc/9878
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25513
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11483
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2819
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17308
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6978
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val611Met
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP

15-38791051-GTGT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791051
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791048
    reference: chr 15
allele count: 1
allele frequency: 8.281985026171072e-6
allele num: 120744
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1709_1711delACA
  hgvsp: ENSP00000452721.1:p.Asn570del
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1709_1711delACA
  hgvsp: ENSP00000388540.2:p.Asn570del
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1250_1615+1252delACA
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*118_*120delACA
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1967_1969delACA
  hgvsp: ENSP00000452859.1:p.Asn656del
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1814_1816delACA
  hgvsp: ENSP00000310244.5:p.Asn605del
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1670_1672delACA
  hgvsp: ENSP00000444762.1:p.Asn557del
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1856_1858delACA
  hgvsp: ENSP00000453583.1:p.Asn619del
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.*45_*47delACA
  variant of: http://identifiers.org/hgnc/9878
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2819
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25528
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17317
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11491
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45056
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1146
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asn605del
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: GTGT
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

15-38791077-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791077
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791077
    reference: chr 15
allele count: 1
allele frequency: 8.280476292996373e-6
allele num: 120766
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*95C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1833C>T
  hgvsp: ENST00000558432.1:c.1833C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1647C>T
  hgvsp: ENST00000539159.1:c.1647C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1686C>T
  hgvsp: ENST00000450598.2:c.1686C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.*22C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1227C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1944C>T
  hgvsp: ENST00000561180.1:c.1944C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1686C>T
  hgvsp: ENST00000559830.1:c.1686C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1791C>T
  hgvsp: ENST00000310803.5:c.1791C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9878
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25544
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11500
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2818
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17313
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asn597Asn
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

15-38791084-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791084
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791084
    reference: chr 15
allele count: 1
allele frequency: 8.280476292996373e-6
allele num: 120766
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1937C>G
  hgvsp: ENSP00000452859.1:p.Ala646Gly
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1679C>G
  hgvsp: ENSP00000452721.1:p.Ala560Gly
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1784C>G
  hgvsp: ENSP00000310244.5:p.Ala595Gly
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1679C>G
  hgvsp: ENSP00000388540.2:p.Ala560Gly
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1640C>G
  hgvsp: ENSP00000444762.1:p.Ala547Gly
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*88C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1220C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.*15C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1826C>G
  hgvsp: ENSP00000453583.1:p.Ala609Gly
  variant of: http://identifiers.org/hgnc/9878
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25542
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17312
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11504
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2819
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 706
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45078
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala595Gly
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

15-38791087-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791087
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791087
    reference: chr 15
allele count: 1
allele frequency: 8.280476292996373e-6
allele num: 120766
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1676G>A
  hgvsp: ENSP00000452721.1:p.Arg559Gln
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1781G>A
  hgvsp: ENSP00000310244.5:p.Arg594Gln
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1934G>A
  hgvsp: ENSP00000452859.1:p.Arg645Gln
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.*12G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1676G>A
  hgvsp: ENSP00000388540.2:p.Arg559Gln
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*85G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1823G>A
  hgvsp: ENSP00000453583.1:p.Arg608Gln
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1637G>A
  hgvsp: ENSP00000444762.1:p.Arg546Gln
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1217G>A
  variant of: http://identifiers.org/hgnc/9878
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2819
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11503
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17311
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25543
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6985
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45078
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg594Gln
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum

15-38791088-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791088
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791088
    reference: chr 15
allele count: 1
allele frequency: 8.280202036929701e-6
allele num: 120770
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.*11C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1780C>G
  hgvsp: ENSP00000310244.5:p.Arg594Gly
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1675C>G
  hgvsp: ENSP00000452721.1:p.Arg559Gly
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1675C>G
  hgvsp: ENSP00000388540.2:p.Arg559Gly
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1822C>G
  hgvsp: ENSP00000453583.1:p.Arg608Gly
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1636C>G
  hgvsp: ENSP00000444762.1:p.Arg546Gly
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1933C>G
  hgvsp: ENSP00000452859.1:p.Arg645Gly
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*84C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1216C>G
  variant of: http://identifiers.org/hgnc/9878
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17310
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11505
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25542
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2819
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1765
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg594Gly
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
population: Latino
reference allele: G
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff

15-38791090-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791090
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791090
    reference: chr 15
allele count: 1
allele frequency: 8.280476292996373e-6
allele num: 120766
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*82A>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1673A>C
  hgvsp: ENSP00000388540.2:p.Lys558Thr
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1931A>C
  hgvsp: ENSP00000452859.1:p.Lys644Thr
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1820A>C
  hgvsp: ENSP00000453583.1:p.Lys607Thr
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1214A>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1634A>C
  hgvsp: ENSP00000444762.1:p.Lys545Thr
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1778A>C
  hgvsp: ENSP00000310244.5:p.Lys593Thr
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1673A>C
  hgvsp: ENSP00000452721.1:p.Lys558Thr
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.*9A>C
  variant of: http://identifiers.org/hgnc/9878
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25542
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17311
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11504
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2820
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Lys593Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

15-38791092-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791092
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791092
    reference: chr 15
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1776G>C
  hgvsp: ENSP00000310244.5:p.Lys592Asn
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1671G>C
  hgvsp: ENSP00000452721.1:p.Lys557Asn
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1818G>C
  hgvsp: ENSP00000453583.1:p.Lys606Asn
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1929G>C
  hgvsp: ENSP00000452859.1:p.Lys643Asn
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1671G>C
  hgvsp: ENSP00000388540.2:p.Lys557Asn
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.*7G>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1212G>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*80G>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1632G>C
  hgvsp: ENSP00000444762.1:p.Lys544Asn
  variant of: http://identifiers.org/hgnc/9878
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2820
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25543
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17311
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11505
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1765
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1536
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Lys592Asn
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD

15-38791108-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791108
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791108
    reference: chr 15
allele count: 1
allele frequency: 8.280202036929701e-6
allele num: 120770
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.363T>C
  hgvsp: ENST00000557875.1:c.363T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1913T>C
  hgvsp: ENSP00000452859.1:p.Val638Ala
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1196T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*64T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1802T>C
  hgvsp: ENSP00000453583.1:p.Val601Ala
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1655T>C
  hgvsp: ENSP00000452721.1:p.Val552Ala
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1655T>C
  hgvsp: ENSP00000388540.2:p.Val552Ala
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1616T>C
  hgvsp: ENSP00000444762.1:p.Val539Ala
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1760T>C
  hgvsp: ENSP00000310244.5:p.Val587Ala
  variant of: http://identifiers.org/hgnc/9878
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17313
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11504
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25543
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2820
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1536
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Val587Ala
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

15-38791142-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791142
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791142
    reference: chr 15
allele count: 1
allele frequency: 8.280202036929701e-6
allele num: 120770
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1726G>A
  hgvsp: ENSP00000310244.5:p.Gly576Arg
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*164G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1621G>A
  hgvsp: ENSP00000388540.2:p.Gly541Arg
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*30G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1768G>A
  hgvsp: ENSP00000453583.1:p.Gly590Arg
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1621G>A
  hgvsp: ENSP00000452721.1:p.Gly541Arg
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1879G>A
  hgvsp: ENSP00000452859.1:p.Gly627Arg
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1162G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.329G>A
  hgvsp: ENSP00000453729.1:p.Arg110Gln
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1582G>A
  hgvsp: ENSP00000444762.1:p.Gly528Arg
  variant of: http://identifiers.org/hgnc/9878
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25542
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2821
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11503
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17312
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1536
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gly576Arg
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

15-38791143-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791143
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791143
    reference: chr 15
allele count: 1
allele frequency: 8.280064915708939e-6
allele num: 120772
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1767C>T
  hgvsp: ENST00000558432.1:c.1767C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1878C>T
  hgvsp: ENST00000561180.1:c.1878C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1725C>T
  hgvsp: ENST00000310803.5:c.1725C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1161C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*163C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1581C>T
  hgvsp: ENST00000539159.1:c.1581C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1620C>T
  hgvsp: ENST00000450598.2:c.1620C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*29C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.328C>T
  hgvsp: ENSP00000453729.1:p.Arg110Trp
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1620C>T
  hgvsp: ENST00000559830.1:c.1620C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9878
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11504
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2820
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17312
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25541
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 707
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg110Trp
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

15-38791152-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791152
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791152
    reference: chr 15
allele count: 1
allele frequency: 8.280339162692104e-6
allele num: 120768
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1721-5C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1763-5C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1152C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1616-5C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*159-5C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.319C>G
  hgvsp: ENSP00000453729.1:p.His107Asp
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1616-5C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*25-5C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1874-5C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1577-5C>G
  variant of: http://identifiers.org/hgnc/9878
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11504
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2820
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25539
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17313
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
hgvs: p.His107Asp
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

15-38791176-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791176
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791176
    reference: chr 15
allele count: 1
allele frequency: 8.282122210995345e-6
allele num: 120742
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1763-29C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*159-29C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1616-29C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1128C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1721-29C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1577-29C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1874-29C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.295C>T
  hgvsp: ENSP00000453729.1:p.Leu99Phe
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*25-29C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1616-29C>T
  variant of: http://identifiers.org/hgnc/9878
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11496
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25516
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17310
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2818
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu99Phe
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

15-38791177-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791177
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791177
    reference: chr 15
allele count: 1
allele frequency: 8.28225940036442e-6
allele num: 120740
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1616-30A>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*25-30A>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.294A>T
  hgvsp: ENSP00000453729.1:p.Arg98Ser
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1721-30A>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1127A>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*159-30A>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1874-30A>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1763-30A>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1616-30A>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1577-30A>T
  variant of: http://identifiers.org/hgnc/9878
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25516
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2818
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11497
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17308
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2693
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg98Ser
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

15-38791177-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791177
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791177
    reference: chr 15
allele count: 1
allele frequency: 8.28225940036442e-6
allele num: 120740
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*159-30A>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1721-30A>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1616-30A>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1763-30A>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.294A>G
  hgvsp: ENST00000557875.1:c.294A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1127A>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1616-30A>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1874-30A>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1577-30A>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*25-30A>G
  variant of: http://identifiers.org/hgnc/9878
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11497
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17308
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25516
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2818
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2693
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Arg98Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum

15-38791178-CTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791178
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791176
    reference: chr 15
allele count: 1
allele frequency: 8.282533792737874e-6
allele num: 120736
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*25-33_*25-32delAA
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*159-33_*159-32delAA
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.291_292delAA
  hgvsp: ENSP00000453729.1:p.Arg98ThrfsTer3
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1616-33_1616-32delAA
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1763-33_1763-32delAA
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1874-33_1874-32delAA
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1616-33_1616-32delAA
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1577-33_1577-32delAA
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1721-33_1721-32delAA
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1124_1615+1125delAA
  variant of: http://identifiers.org/hgnc/9878
canonical: false
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2818
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17309
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25514
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11497
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg98ThrfsTer3
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: CTT
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

15-38791191-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791191
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791191
    reference: chr 15
allele count: 1
allele frequency: 8.287338604080686e-6
allele num: 120666
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*159-44G>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.280G>C
  hgvsp: ENSP00000453729.1:p.Glu94Gln
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1113G>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1577-44G>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1874-44G>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1616-44G>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1763-44G>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1721-44G>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*25-44G>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1616-44G>C
  variant of: http://identifiers.org/hgnc/9878
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11473
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2816
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17296
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Glu94Gln
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
reference allele: C
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/15-38791197-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791197
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791197
    reference: chr 15
allele count: 1
allele frequency: 8.291461452995706e-6
allele num: 120606
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.274G>T
  hgvsp: ENSP00000453729.1:p.Gly92Ter
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1721-50G>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1874-50G>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1616-50G>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*159-50G>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*25-50G>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1763-50G>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1616-50G>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1577-50G>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1107G>T
  variant of: http://identifiers.org/hgnc/9878
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17278
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2815
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11466
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25426
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly92Ter
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

15-38791217-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791217
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791217
    reference: chr 15
allele count: 1
allele frequency: 8.314901967305805e-6
allele num: 120266
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1763-70T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1616-70T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.254T>C
  hgvsp: ENSP00000453729.1:p.Phe85Ser
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*159-70T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1616-70T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1874-70T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1577-70T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1721-70T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*25-70T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1087T>C
  variant of: http://identifiers.org/hgnc/9878
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2813
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17149
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11403
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25247
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Phe85Ser
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

15-38791218-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791218
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791218
    reference: chr 15
allele count: 1
allele frequency: 8.3166999334664e-6
allele num: 120240
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1874-71T>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.253T>A
  hgvsp: ENSP00000453729.1:p.Phe85Ile
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*159-71T>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1577-71T>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1086T>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1763-71T>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1721-71T>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*25-71T>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1616-71T>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1616-71T>A
  variant of: http://identifiers.org/hgnc/9878
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25236
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17131
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11401
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2813
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44636
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Phe85Ile
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD

15-38791221-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791221
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791221
    reference: chr 15
allele count: 1
allele frequency: 8.321821480285606e-6
allele num: 120166
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1874-74G>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1616-74G>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1577-74G>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1721-74G>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.250G>C
  hgvsp: ENSP00000453729.1:p.Glu84Gln
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1763-74G>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*25-74G>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1616-74G>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1083G>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*159-74G>C
  variant of: http://identifiers.org/hgnc/9878
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2808
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25189
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11391
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17080
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1499
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu84Gln
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

15-38791237-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791237
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791237
    reference: chr 15
allele count: 3
allele frequency: 2.514964036014285e-5
allele num: 119286
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1874-90C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*25-90C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1721-90C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.234C>G
  hgvsp: ENSP00000453729.1:p.Asp78Glu
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*159-90C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1763-90C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1616-90C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1616-90C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1067C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1577-90C>G
  variant of: http://identifiers.org/hgnc/9878
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11275
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16647
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24749
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2685
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 6710
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1479
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Asp78Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

15-38791243-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791243
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791243
    reference: chr 15
allele count: 18
allele frequency: 1.513800817452441e-4
allele num: 118906
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1616-96G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*25-96G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1721-96G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1874-96G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*159-96G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1061G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1763-96G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1616-96G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1577-96G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.228G>A
  hgvsp: ENSP00000453729.1:p.Met76Ile
  variant of: http://identifiers.org/hgnc/9878
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16391
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24601
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11204
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2774
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Met76Ile
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

15-38791243-CAT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791243
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791241
    reference: chr 15
allele count: 34
allele frequency: 2.859401544076834e-4
allele num: 118906
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1721-98_1721-97delAT
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.226_227delAT
  hgvsp: ENSP00000453729.1:p.Met76ValfsTer2
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1763-98_1763-97delAT
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1616-98_1616-97delAT
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1577-98_1577-97delAT
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*159-98_*159-97delAT
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*25-98_*25-97delAT
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1874-98_1874-97delAT
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1059_1615+1060delAT
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1616-98_1616-97delAT
  variant of: http://identifiers.org/hgnc/9878
canonical: false
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11204
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2774
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16391
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 24601
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Met76ValfsTer2
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: CAT
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

15-38791244-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791244
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791244
    reference: chr 15
allele count: 1
allele frequency: 8.414250374434141e-6
allele num: 118846
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*25-97T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1874-97T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.227T>C
  hgvsp: ENSP00000453729.1:p.Met76Thr
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1721-97T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1616-97T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1060T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*159-97T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1616-97T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1763-97T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1577-97T>C
  variant of: http://identifiers.org/hgnc/9878
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24610
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2774
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16399
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11204
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Met76Thr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD

15-38791250-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791250
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791250
    reference: chr 15
allele count: 12
allele frequency: 1.014576076296121e-4
allele num: 118276
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1721-103C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1616-103C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.221C>G
  hgvsp: ENSP00000453729.1:p.Thr74Arg
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1054C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1763-103C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1616-103C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1874-103C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1577-103C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*25-103C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*159-103C>G
  variant of: http://identifiers.org/hgnc/9878
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24445
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11146
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2736
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 4.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2221
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1447
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Thr74Arg
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: QD

15-38791253-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791253
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791253
    reference: chr 15
allele count: 1
allele frequency: 8.48219587086705e-6
allele num: 117894
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1874-106G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1763-106G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1616-106G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1721-106G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*159-106G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1616-106G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1051G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.218G>A
  hgvsp: ENSP00000453729.1:p.Arg73Lys
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1577-106G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*25-106G>A
  variant of: http://identifiers.org/hgnc/9878
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2729
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24372
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11090
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15660
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1444
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg73Lys
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

15-38791255-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791255
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791255
    reference: chr 15
allele count: 2
allele frequency: 1.700767045937718e-5
allele num: 117594
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1763-108T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1616-108T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.216T>C
  hgvsp: ENST00000557875.1:c.216T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*25-108T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1721-108T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1577-108T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1049T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*159-108T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1874-108T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1616-108T>C
  variant of: http://identifiers.org/hgnc/9878
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24273
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11058
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15387
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2722
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asp72Asp
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS

15-38791256-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791256
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791256
    reference: chr 15
allele count: 1
allele frequency: 8.513826454161559e-6
allele num: 117456
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1577-109A>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1048A>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1874-109A>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1763-109A>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1616-109A>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*25-109A>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*159-109A>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1616-109A>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1721-109A>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.215A>C
  hgvsp: ENSP00000453729.1:p.Asp72Ala
  variant of: http://identifiers.org/hgnc/9878
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11049
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24208
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15262
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2723
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1441
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Asp72Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ

15-38791260-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791260
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791260
    reference: chr 15
allele count: 1
allele frequency: 8.568833439015613e-6
allele num: 116702
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1763-113G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1044G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1616-113G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*159-113G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.211G>A
  hgvsp: ENSP00000453729.1:p.Glu71Lys
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1721-113G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*25-113G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1874-113G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1577-113G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1616-113G>A
  variant of: http://identifiers.org/hgnc/9878
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2717
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2374
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14665
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1776
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23990
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10946
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1424
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Glu71Lys
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
population: African
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum

15-38791269-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791269
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791269
    reference: chr 15
allele count: 92
allele frequency: 8.051247943431232e-4
allele num: 114268
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1874-122T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1577-122T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*25-122T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1721-122T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1616-122T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1035T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.202T>C
  hgvsp: ENST00000557875.1:c.202T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*159-122T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1616-122T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1763-122T>C
  variant of: http://identifiers.org/hgnc/9878
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 23060
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10538
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2759
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3442
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 4.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 2655
  bin: 3.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13067
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 5.25e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5523
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1610
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Leu68Leu
num of homozygotes: 1
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

15-38791279-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791279
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791279
    reference: chr 15
allele count: 1
allele frequency: 9.171955827860732e-6
allele num: 109028
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1763-132G>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1577-132G>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1025G>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1616-132G>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.192G>C
  hgvsp: ENSP00000453729.1:p.Met64Ile
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1721-132G>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*159-132G>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*25-132G>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1874-132G>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1616-132G>C
  variant of: http://identifiers.org/hgnc/9878
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2469
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5340
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4821
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11861
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20847
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9282
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1035
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1030
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Met64Ile
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

15-38791283-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791283
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791283
    reference: chr 15
allele count: 14328
allele frequency: 1.369344572509892e-1
allele num: 104634
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1721-136G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1021G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*25-136G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1616-136G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1763-136G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1874-136G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.188G>A
  hgvsp: ENSP00000453729.1:p.Gly63Glu
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1577-136G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*159-136G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1616-136G>A
  variant of: http://identifiers.org/hgnc/9878
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.75e1
  variant carriers: 206
genotype depth: GenotypeDepth
  all individuals: 9911
  bin: 2.25e1
  variant carriers: 1412
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 2.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 4.75e1
  variant carriers: 754
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 8.75e1
  variant carriers: 142
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 9.75e1
  variant carriers: 431
genotype depth: GenotypeDepth
  all individuals: 6947
  bin: 1.25e1
  variant carriers: 577
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 237
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 122
genotype depth: GenotypeDepth
  all individuals: 6422
  bin: 7.5e0
  variant carriers: 261
genotype depth: GenotypeDepth
  all individuals: 2128
  bin: 1.75e1
  variant carriers: 971
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 3.75e1
  variant carriers: 1794
genotype depth: GenotypeDepth
  all individuals: 18406
  bin: 2.75e1
  variant carriers: 1971
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 5.25e1
  variant carriers: 490
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 175
genotype depth: GenotypeDepth
  all individuals: 8040
  bin: 3.25e1
  variant carriers: 2008
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 4.25e1
  variant carriers: 1172
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 6.25e1
  variant carriers: 261
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.75e1
  variant carriers: 380
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.25e1
  variant carriers: 188
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 4.25e1
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 7.75e1
  variant carriers: 106
genotype quality: GenotypeQuality
  all individuals: 751
  bin: 2.75e1
  variant carriers: 24
hgvs: p.Gly63Glu
num of homozygotes: 1084
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

15-38791287-ATGAAGCTAGCATTCTTCTCACTTGG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791287
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791262
    reference: chr 15
allele count: 1
allele frequency: 1.024569168664577e-5
allele num: 97602
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsp: ENSP00000453729.1:p.Gln54Ter
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  variant of: http://identifiers.org/hgnc/9878
canonical: false
consequence: frameshift
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20303
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1842
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9527
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9541
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6793
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9872
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gln54Ter
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: ATGAAGCTAGCATTCTTCTCACTTGG
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

15-38791300-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791300
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791300
    reference: chr 15
allele count: 1
allele frequency: 1.244493117953058e-5
allele num: 80354
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1577-153A>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1721-153A>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1874-153A>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+1004A>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1763-153A>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.171A>G
  hgvsp: ENST00000557875.1:c.171A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*25-153A>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1616-153A>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*159-153A>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1616-153A>G
  variant of: http://identifiers.org/hgnc/9878
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2847
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2417
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3872
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14881
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8254
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15704
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11675
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4168
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 883
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1695
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg57Arg
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/15-38791307-AC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791307
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791306
    reference: chr 15
allele count: 2
allele frequency: 2.774848770741995e-5
allele num: 72076
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1616-161delG
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1577-161delG
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1721-161delG
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*25-161delG
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1874-161delG
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1763-161delG
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.163delG
  hgvsp: ENSP00000453729.1:p.Val55Ter
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1616-161delG
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+996delG
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*159-161delG
  variant of: http://identifiers.org/hgnc/9878
canonical: false
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16527
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2356
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5269
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7065
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8303
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5583
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Val55Ter
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: AC
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

15-38791312-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791312
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791312
    reference: chr 15
allele count: 1
allele frequency: 1.541544627716972e-5
allele num: 64870
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1763-165C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1577-165C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1721-165C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*159-165C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*25-165C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1616-165C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+992C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.159C>T
  hgvsp: ENST00000557875.1:c.159C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1874-165C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1616-165C>T
  variant of: http://identifiers.org/hgnc/9878
canonical: false
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19677
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2198
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6957
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16800
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6240
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6184
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 328
  bin: 5.75e1
  variant carriers: 0
hgvs: p.His53His
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

15-38791314-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791314
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791314
    reference: chr 15
allele count: 3
allele frequency: 4.79877151449229e-5
allele num: 62516
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+990C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1763-167C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1721-167C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*25-167C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*159-167C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1616-167C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1874-167C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.157C>T
  hgvsp: ENSP00000453729.1:p.His53Tyr
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1577-167C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1616-167C>T
  variant of: http://identifiers.org/hgnc/9878
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16726
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2123
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20081
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6047
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5577
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7603
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1262
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 9.75e1
  variant carriers: 3
hgvs: p.His53Tyr
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

15-38791319-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791319
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791319
    reference: chr 15
allele count: 15
allele frequency: 2.606882168925965e-4
allele num: 57540
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1874-172G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+985G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1721-172G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1577-172G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*159-172G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.152G>A
  hgvsp: ENSP00000453729.1:p.Gly51Glu
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1616-172G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*25-172G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1616-172G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1763-172G>A
  variant of: http://identifiers.org/hgnc/9878
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4503
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20728
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1869
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5557
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 9202
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16292
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 905
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 9.25e1
  variant carriers: 2
hgvs: p.Gly51Glu
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

15-38791324-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791324
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791324
    reference: chr 15
allele count: 61
allele frequency: 1.12808373710101e-3
allele num: 54074
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1616-177C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*159-177C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*25-177C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1577-177C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+980C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1763-177C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.147C>G
  hgvsp: ENSP00000453729.1:p.Ser49Arg
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1616-177C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1874-177C>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1721-177C>G
  variant of: http://identifiers.org/hgnc/9878
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10512
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3904
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21118
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1602
  bin: 1.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 5148
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15777
  bin: 1.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 742
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1425
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser49Arg
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQRankSum

15-38791329-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791329
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791329
    reference: chr 15
allele count: 1
allele frequency: 2.050777244575694e-5
allele num: 48762
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1616-182G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+975G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1763-182G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*25-182G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.142G>A
  hgvsp: ENSP00000453729.1:p.Val48Met
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1721-182G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*159-182G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1616-182G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1874-182G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1577-182G>A
  variant of: http://identifiers.org/hgnc/9878
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14854
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3258
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13028
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1422
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4374
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20874
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13711
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 877
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val48Met
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/15-38791330-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791330
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791330
    reference: chr 15
allele count: 1
allele frequency: 2.119362495761275e-5
allele num: 47184
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*25-183T>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1616-183T>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1874-183T>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.141T>G
  hgvsp: ENSP00000453729.1:p.Ser47Arg
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1763-183T>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+974T>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1721-183T>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1616-183T>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*159-183T>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1577-183T>G
  variant of: http://identifiers.org/hgnc/9878
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14644
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20789
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13478
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4268
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3164
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6740
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1746
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1179
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser47Arg
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum

http://identifiers.org/exac.variant/15-38791345-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791345
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791345
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 33066
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1874-198G>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1763-198G>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1721-198G>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*25-198G>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1616-198G>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1616-198G>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1577-198G>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.126G>T
  hgvsp: ENSP00000453729.1:p.Lys42Asn
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+959G>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*159-198G>T
  variant of: http://identifiers.org/hgnc/9878
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10019
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18634
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21259
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3287
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2059
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22181
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22130
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Lys42Asn
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

15-38791347-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791347
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791347
    reference: chr 15
allele count: 1
allele frequency: 3.217503217503217e-5
allele num: 31080
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1763-200A>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1616-200A>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1616-200A>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*159-200A>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1721-200A>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1874-200A>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*25-200A>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.124A>G
  hgvsp: ENSP00000453729.1:p.Lys42Glu
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+957A>G
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1577-200A>G
  variant of: http://identifiers.org/hgnc/9878
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3130
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9310
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17868
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22684
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1168
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 988
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Lys42Glu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

15-38791348-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791348
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791348
    reference: chr 15
allele count: 1748
allele frequency: 5.716902145473574e-2
allele num: 30576
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1616-201T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+956T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*25-201T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1721-201T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1616-201T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1874-201T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*159-201T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.123T>C
  hgvsp: ENST00000557875.1:c.123T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1577-201T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1763-201T>C
  variant of: http://identifiers.org/hgnc/9878
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 1.75e1
  variant carriers: 275
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 3.75e1
  variant carriers: 82
genotype depth: GenotypeDepth
  all individuals: 17733
  bin: 7.5e0
  variant carriers: 1097
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2922
  bin: 2.25e1
  variant carriers: 153
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 3.25e1
  variant carriers: 101
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22869
  bin: 2.5e0
  variant carriers: 150
genotype depth: GenotypeDepth
  all individuals: 9039
  bin: 1.25e1
  variant carriers: 742
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 2.75e1
  variant carriers: 104
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.25e1
  variant carriers: 57
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 23257
  bin: 7.5e0
  variant carriers: 59
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 8.75e1
  variant carriers: 120
genotype quality: GenotypeQuality
  all individuals: 4194
  bin: 6.25e1
  variant carriers: 46
hgvs: p.Asp41Asp
num of homozygotes: 152
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD

15-38791351-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791351
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791351
    reference: chr 15
allele count: 1
allele frequency: 3.950383187169155e-5
allele num: 25314
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1616-204T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1763-204T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*25-204T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1616-204T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*159-204T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.120T>C
  hgvsp: ENST00000557875.1:c.120T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+953T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1874-204T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1721-204T>C
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1577-204T>C
  variant of: http://identifiers.org/hgnc/9878
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26279
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16326
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7378
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2663
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26750
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1186
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr40Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

15-38791369-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791369
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791369
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 15016
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1616-222T>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1763-222T>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1874-222T>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1721-222T>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.102T>A
  hgvsp: ENST00000557875.1:c.102T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1577-222T>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*159-222T>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+935T>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1616-222T>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*25-222T>A
  variant of: http://identifiers.org/hgnc/9878
canonical: false
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32222
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11711
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 513
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31919
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu34Leu
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS

15-38791386-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791386
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791386
    reference: chr 15
allele count: 1
allele frequency: 1.01461038961039e-4
allele num: 9856
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1874-239G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*25-239G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1577-239G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*159-239G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.86-1G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1616-239G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1763-239G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1721-239G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1616-239G>A
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+918G>A
  variant of: http://identifiers.org/hgnc/9878
canonical: false
consequence: splice acceptor
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7796
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32911
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3316
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  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: 395
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
hgvs: c.86-1G>A
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP

15-38791393-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791393
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791393
    reference: chr 15
allele count: 63
allele frequency: 7.368421052631579e-3
allele num: 8550
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*159-246C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1874-246C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1577-246C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+911C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.86-8C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1763-246C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1721-246C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*25-246C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1616-246C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1616-246C>T
  variant of: http://identifiers.org/hgnc/9878
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6866
  bin: 7.5e0
  variant carriers: 160
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 1.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 1.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 32053
  bin: 2.5e0
  variant carriers: 76
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 503
  bin: 3.25e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 3.75e1
  variant carriers: 0
hgvs: c.86-8C>T
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

15-38791411-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 38791411
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 38791411
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 6248
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452721
  ensembl transcript: ENST00000559830
  gene symbol: RASGRP1
  hgvsc: ENST00000559830.1:c.1616-264C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000413105
  ensembl transcript: ENST00000414708
  gene symbol: RASGRP1
  hgvsc: ENST00000414708.2:c.*25-264C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454053
  ensembl transcript: ENST00000560425
  gene symbol: RASGRP1
  hgvsc: ENST00000560425.1:c.*159-264C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453583
  ensembl transcript: ENST00000558432
  gene symbol: RASGRP1
  hgvsc: ENST00000558432.1:c.1763-264C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000452859
  ensembl transcript: ENST00000561180
  gene symbol: RASGRP1
  hgvsc: ENST00000561180.1:c.1874-264C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000453729
  ensembl transcript: ENST00000557875
  gene symbol: RASGRP1
  hgvsc: ENST00000557875.1:c.86-26C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000454164
  ensembl transcript: ENST00000558164
  gene symbol: RASGRP1
  hgvsc: ENST00000558164.1:c.1615+893C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000310244
  ensembl transcript: ENST00000310803
  gene symbol: RASGRP1
  hgvsc: ENST00000310803.5:c.1721-264C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000444762
  ensembl transcript: ENST00000539159
  gene symbol: RASGRP1
  hgvsc: ENST00000539159.1:c.1577-264C>T
  variant of: http://identifiers.org/hgnc/9878
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172575
  ensembl protein: ENSP00000388540
  ensembl transcript: ENST00000450598
  gene symbol: RASGRP1
  hgvsc: ENST00000450598.2:c.1616-264C>T
  variant of: http://identifiers.org/hgnc/9878
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30723
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2371
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5756
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25642
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4641
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: DP

GenotypeQuality
all individuals: 223
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 812
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1008
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3510
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5130
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7925
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6160
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2525
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1036
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2602
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1510
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5487
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7684
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5296
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.923722828219414e-5
allele num: 50972
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5722
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8470
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.359e0

FS
type: SiteQuality
SIO_000300: 8.371e0

VQSLOD
type: SiteQuality
SIO_000300: -8.331e-1

QD
type: SiteQuality
SIO_000300: 7.59e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 8.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

DP
type: SiteQuality
SIO_000300: 8.3794e5

ClippingRankSum
type: SiteQuality
SIO_000300: -1.43e-1

GenotypeQuality
all individuals: 1551
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2537
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4734
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 715
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7923
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11158
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1122
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3547
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2542
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 994
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2287
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4265
bin: 1.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6502
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 5.289139633286319e-4
allele num: 5672
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5228
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7616
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50386
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8336
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 596
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.6e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.615e1

VQSLOD
type: SiteQuality
SIO_000300: 1.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 7.572e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.262e0

DP
type: SiteQuality
SIO_000300: 8.38234e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.71e-1

GenotypeQuality
all individuals: 1749
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1154
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 844
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 695
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1314
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1438
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2713
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1453
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35470
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1433
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 2.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8386
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14420
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9720
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.533836431682925e-5
allele num: 65196
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.162e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 6.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.39e-1

QD
type: SiteQuality
SIO_000300: 1.237e1

VQSLOD
type: SiteQuality
SIO_000300: 4.36e0

DP
type: SiteQuality
SIO_000300: 1.611429e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.492e0

MQ
type: SiteQuality
SIO_000300: 5.506e1

GenotypeQuality
all individuals: 824
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 594
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2698
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1429
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6446
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1406
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1264
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 689
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1679
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1093
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 742
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9728
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65304
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8400
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.873797085510036e-5
allele num: 14548
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11446
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.062e0

QD
type: SiteQuality
SIO_000300: 1.497e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.28e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.09e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.19e-1

DP
type: SiteQuality
SIO_000300: 1.618166e6

VQSLOD
type: SiteQuality
SIO_000300: -9.644e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.65e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.4e-3

GenotypeQuality
all individuals: 99
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1079
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39099
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1694
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 769
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6474
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 538
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1301
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1670
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 689
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 686
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1415
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.854949273375377e-5
allele num: 14588
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8406
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9734
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65320
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.96e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.17e0

QD
type: SiteQuality
SIO_000300: 1.074e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.62948e6

MQRankSum
type: SiteQuality
SIO_000300: 1.44e-1

GenotypeQuality
all individuals: 54
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40038
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1418
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2692
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 684
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1071
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1690
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 966
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6499
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.825006825006825e-5
allele num: 14652
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65408
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11470
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9738
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8418
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

QD
type: SiteQuality
SIO_000300: 2.067e1

MQ
type: SiteQuality
SIO_000300: 5.946e1

DP
type: SiteQuality
SIO_000300: 1.637285e6

FS
type: SiteQuality
SIO_000300: 3.302e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.44e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.56e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.291e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.558e0

GenotypeQuality
all individuals: 1414
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1667
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 110
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6488
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 686
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40255
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1645
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1068
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 449
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8412
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9736
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65386
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.832467887400929e-5
allele num: 14636
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.75e-1

QD
type: SiteQuality
SIO_000300: 1.965e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.66e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.98e0

MQ
type: SiteQuality
SIO_000300: 5.948e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.9e-3

FS
type: SiteQuality
SIO_000300: 3.287e0

DP
type: SiteQuality
SIO_000300: 1.64045e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.737e0

VQSLOD
type: SiteQuality
SIO_000300: -1.896e0

GenotypeQuality
all individuals: 497
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6591
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41637
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1426
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 568
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
all individuals: 161
bin: 4.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9752
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.18427285646613e-4
allele num: 8444
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14820
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65584
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.29e0

DP
type: SiteQuality
SIO_000300: 1.655435e6

FS
type: SiteQuality
SIO_000300: 6.222e0

MQ
type: SiteQuality
SIO_000300: 5.911e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.6e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.2e-3

QD
type: SiteQuality
SIO_000300: 1.366e1

VQSLOD
type: SiteQuality
SIO_000300: -3.508e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.53e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8462
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14966
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9756
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.046922608165752e-5
allele num: 65640
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.43e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.59e0

MQRankSum
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SIO_000300: 6.74e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.315e1

DP
type: SiteQuality
SIO_000300: 1.659621e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.71e-1

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.04062271953296e-5
allele num: 65776
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8484
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15124
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9762
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 7.687e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.184e1

MQRankSum
type: SiteQuality
SIO_000300: -3.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.313e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.32e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.32e-1

DP
type: SiteQuality
SIO_000300: 1.666617e6

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15304
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.175364362952515e-4
allele num: 8508
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9768
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65920
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.0e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.43e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -5.302e0

QD
type: SiteQuality
SIO_000300: 1.146e1

DP
type: SiteQuality
SIO_000300: 1.671875e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.96e-1

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.51437138443832e-5
allele num: 66034
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9770
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.92e-1

QD
type: SiteQuality
SIO_000300: 1.57e1

MQRankSum
type: SiteQuality
SIO_000300: -1.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.64e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

FS
type: SiteQuality
SIO_000300: 2.1e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 8.06e-1

DP
type: SiteQuality
SIO_000300: 1.678897e6

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

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

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

South Asian
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allele count: 1
allele frequency: 6.372673973999491e-5
allele num: 15692
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66132
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9780
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.76e-1

InbreedingCoeff
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.872e1

DP
type: SiteQuality
SIO_000300: 1.683501e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66520
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.108735491753207e-5
allele num: 16370
num of homozygotes: 0

MQRankSum
type: SiteQuality
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BaseQRankSum
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.726e1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16418
num of homozygotes: 0

Latino
type: Population
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allele frequency: 8.646031471554557e-5
allele num: 11566
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: 6614
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66574
num of homozygotes: 0

East Asian
type: Population
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Other
type: Population
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num of homozygotes: 0

FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
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ClippingRankSum
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DP
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InbreedingCoeff
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MQ
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 9

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

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

South Asian
type: Population
allele count: 4
allele frequency: 2.426595486532395e-4
allele num: 16484
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.000840235265874e-5
allele num: 66648
num of homozygotes: 0

African
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allele count: 2
allele frequency: 2.040399918384003e-4
allele num: 9802
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.99e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.75e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.89e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.4e-3

QD
type: SiteQuality
SIO_000300: 1.676e1

VQSLOD
type: SiteQuality
SIO_000300: 7.89e-1

DP
type: SiteQuality
SIO_000300: 1.707398e6

MQRankSum
type: SiteQuality
SIO_000300: -3.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.06e-1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499880009599232e-5
allele num: 66672
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

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

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

Latino
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allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.973e1

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.245e0

VQSLOD
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ClippingRankSum
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SIO_000300: 2.4e-2

BaseQRankSum
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SIO_000300: -7.617e0

DP
type: SiteQuality
SIO_000300: 1.707306e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.71e-1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66690
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

African
type: Population
allele count: 1
allele frequency: 1.020199959192002e-4
allele num: 9802
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.8e-1

QD
type: SiteQuality
SIO_000300: 1.599e1

VQSLOD
type: SiteQuality
SIO_000300: -9.267e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.5e-2

BaseQRankSum
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SIO_000300: -1.032e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.0e-1

FS
type: SiteQuality
SIO_000300: 1.0483e1

MQ
type: SiteQuality
SIO_000300: 5.988e1

DP
type: SiteQuality
SIO_000300: 1.708151e6

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66694
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
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: 2
allele frequency: 1.211680600993578e-4
allele num: 16506
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.591e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.1e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e0

FS
type: SiteQuality
SIO_000300: 6.608e0

MQ
type: SiteQuality
SIO_000300: 5.984e1

DP
type: SiteQuality
SIO_000300: 1.708331e6

MQRankSum
type: SiteQuality
SIO_000300: 1.64e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.65e0

QD
type: SiteQuality
SIO_000300: 1.462e1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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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: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 1.020199959192002e-4
allele num: 9802
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.62e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.674e0

VQSLOD
type: SiteQuality
SIO_000300: 9.71e-1

FS
type: SiteQuality
SIO_000300: 2.163e0

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.367e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

MQ
type: SiteQuality
SIO_000300: 5.988e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.987e0

DP
type: SiteQuality
SIO_000300: 1.708487e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.964e0

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.824e1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11576
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
allele num: 16512
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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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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Latino
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European (Non-Finnish)
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
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FS
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InbreedingCoeff
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MQRankSum
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MQ
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

East Asian
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allele num: 8624
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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Latino
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allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

European (Finnish)
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African
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allele frequency: 1.020199959192002e-4
allele num: 9802
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
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MQ
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ReadPosRankSum
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DP
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FS
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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QD
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MQRankSum
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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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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 num: 66740
num of homozygotes: 0

African
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allele frequency: 0.0e0
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Other
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East Asian
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South Asian
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Latino
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allele frequency: 0.0e0
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FS
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QD
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VQSLOD
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ClippingRankSum
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MQ
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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DP
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Other
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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African
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East Asian
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South Asian
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DP
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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FS
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QD
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MQ
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 num: 66740
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
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East Asian
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Other
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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QD
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DP
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MQ
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BaseQRankSum
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ClippingRankSum
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SIO_000300: 9.379999999999999e-1

FS
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VQSLOD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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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: 16512
num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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Latino
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African
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European (Non-Finnish)
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South Asian
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InbreedingCoeff
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FS
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ClippingRankSum
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BaseQRankSum
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MQ
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MQRankSum
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ReadPosRankSum
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DP
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VQSLOD
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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East Asian
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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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Other
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MQRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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MQ
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DP
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele num: 11576
num of homozygotes: 0

Other
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African
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South Asian
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East Asian
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European (Non-Finnish)
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European (Finnish)
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MQRankSum
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InbreedingCoeff
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FS
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VQSLOD
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MQ
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QD
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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Other
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Latino
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East Asian
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European (Finnish)
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European (Non-Finnish)
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InbreedingCoeff
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SIO_000300: 5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -7.084e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.25e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.6e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e-1

DP
type: SiteQuality
SIO_000300: 1.708947e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.6e-1

QD
type: SiteQuality
SIO_000300: 1.246e1

GenotypeQuality
all individuals: 1529
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 707
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6975
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -2.93e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 6.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

MQRankSum
type: SiteQuality
SIO_000300: 1.53e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.352e0

QD
type: SiteQuality
SIO_000300: 1.083e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.0e-2

DP
type: SiteQuality
SIO_000300: 1.70894e6

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 1.020199959192002e-4
allele num: 9802
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.083e1

VQSLOD
type: SiteQuality
SIO_000300: -2.93e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.53e0

DP
type: SiteQuality
SIO_000300: 1.70894e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

FS
type: SiteQuality
SIO_000300: 6.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.352e0

GenotypeQuality
all individuals: 30
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 45061
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
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: 898
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
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: 1.498890820792613e-5
allele num: 66716
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.932e0

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.89e-1

QD
type: SiteQuality
SIO_000300: 1.775e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.4e-1

MQ
type: SiteQuality
SIO_000300: 5.983e1

DP
type: SiteQuality
SIO_000300: 1.70892e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.03e-1

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

GenotypeQuality
all individuals: 44981
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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: 2.75e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 1135
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66678
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9778
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.932e1

QD
type: SiteQuality
SIO_000300: 1.614e1

FS
type: SiteQuality
SIO_000300: 3.254e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.67e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 9.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.14e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.37e-1

DP
type: SiteQuality
SIO_000300: 1.707353e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.75e-1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.646031471554557e-5
allele num: 11566
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66642
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9768
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.586e0

DP
type: SiteQuality
SIO_000300: 1.706345e6

QD
type: SiteQuality
SIO_000300: 1.554e1

VQSLOD
type: SiteQuality
SIO_000300: 4.53e-1

FS
type: SiteQuality
SIO_000300: 2.255e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.464e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.16e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9690
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505072092953252e-5
allele num: 66442
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 7.24e0

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e0

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.700411e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -8.169999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.42e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9684
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.664009703690868e-5
allele num: 11542
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66422
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 4.55e-1

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 2.51e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.79e-1

FS
type: SiteQuality
SIO_000300: 4.551e0

DP
type: SiteQuality
SIO_000300: 1.699923e6

MQ
type: SiteQuality
SIO_000300: 5.943e1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.394e1

GenotypeQuality
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variant carriers: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9668
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66372
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.896e0

QD
type: SiteQuality
SIO_000300: 1.423e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-2

DP
type: SiteQuality
SIO_000300: 1.698273e6

GenotypeQuality
all individuals: 20
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1321
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 43681
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1697
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1112
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 702
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65826
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8504
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.161888701517706e-4
allele num: 9488
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16480
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.68334e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.47e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.89e-1

QD
type: SiteQuality
SIO_000300: 1.793e1

VQSLOD
type: SiteQuality
SIO_000300: -2.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 5.27e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -7.8e-2

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

GenotypeQuality
all individuals: 142
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1104
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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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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variant carriers: 0

GenotypeQuality
all individuals: 1690
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2721
bin: 9.75e1
variant carriers: 18

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9412
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8452
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11482
num of homozygotes: 0

South Asian
type: Population
allele count: 18
allele frequency: 1.092498179169701e-3
allele num: 16476
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

FS
type: SiteQuality
SIO_000300: 8.05e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.88e-1

DP
type: SiteQuality
SIO_000300: 1.678252e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.458e0

MQ
type: SiteQuality
SIO_000300: 6.015e1

QD
type: SiteQuality
SIO_000300: 1.631e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.87e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.93e0

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

GenotypeQuality
all individuals: 43299
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1470
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2721
bin: 9.75e1
variant carriers: 34

GenotypeQuality
all individuals: 30
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variant carriers: 0

GenotypeQuality
all individuals: 1104
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 24
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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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 701
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 3.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 8
allele frequency: 4.855547462976451e-4
allele num: 16476
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9412
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.709284096847239e-5
allele num: 11482
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.04905936518584e-5
allele num: 65594
num of homozygotes: 0

East Asian
type: Population
allele count: 23
allele frequency: 2.721249408424042e-3
allele num: 8452
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

MQ
type: SiteQuality
SIO_000300: 6.015e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.1e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.87e-1

FS
type: SiteQuality
SIO_000300: 8.05e-1

QD
type: SiteQuality
SIO_000300: 1.631e1

VQSLOD
type: SiteQuality
SIO_000300: 3.93e0

MQRankSum
type: SiteQuality
SIO_000300: 2.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.458e0

DP
type: SiteQuality
SIO_000300: 1.678252e6

GenotypeQuality
all individuals: 25
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6648
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1690
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variant carriers: 0

GenotypeQuality
all individuals: 105
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GenotypeQuality
all individuals: 2672
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variant carriers: 1

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 26
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variant carriers: 0

GenotypeQuality
all individuals: 29
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variant carriers: 0

GenotypeQuality
all individuals: 12
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GenotypeQuality
all individuals: 144
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GenotypeQuality
all individuals: 43347
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1104
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
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variant carriers: 0

GenotypeQuality
all individuals: 701
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8406
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.524436720631727e-5
allele num: 65598
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9416
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.954e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.092e0

MQRankSum
type: SiteQuality
SIO_000300: 7.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.11e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

DP
type: SiteQuality
SIO_000300: 1.674799e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.746e1

VQSLOD
type: SiteQuality
SIO_000300: 1.44e-1

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

GenotypeQuality
all individuals: 6544
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variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 211
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variant carriers: 0

GenotypeQuality
all individuals: 1676
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 13
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GenotypeQuality
all individuals: 1096
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 699
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GenotypeQuality
all individuals: 2677
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variant carriers: 12

GenotypeQuality
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GenotypeQuality
all individuals: 42740
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variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 3
allele frequency: 2.624671916010499e-4
allele num: 11430
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8392
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.075500107550011e-4
allele num: 9298
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.226880961874674e-4
allele num: 65206
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.3e0

DP
type: SiteQuality
SIO_000300: 1.665355e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.93e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.15e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.622e1

GenotypeQuality
all individuals: 27
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2570
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variant carriers: 0

GenotypeQuality
all individuals: 447
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GenotypeQuality
all individuals: 2669
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variant carriers: 1

GenotypeQuality
all individuals: 42299
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GenotypeQuality
all individuals: 240
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 112
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6508
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variant carriers: 0

GenotypeQuality
all individuals: 1096
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11392
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8370
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64964
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.082251082251082e-4
allele num: 9240
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.884e0

VQSLOD
type: SiteQuality
SIO_000300: -2.649e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 1.658341e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.4e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.42e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.062e0

QD
type: SiteQuality
SIO_000300: 2.856e1

GenotypeQuality
all individuals: 118
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1666
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variant carriers: 0

GenotypeQuality
all individuals: 52
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GenotypeQuality
all individuals: 213
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GenotypeQuality
all individuals: 14
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GenotypeQuality
all individuals: 43
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GenotypeQuality
all individuals: 447
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 6481
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variant carriers: 0

GenotypeQuality
all individuals: 699
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8334
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.77963125548727e-5
allele num: 11390
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9204
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64760
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.084945843981989e-5
allele num: 16434
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.73e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.39e0

VQSLOD
type: SiteQuality
SIO_000300: 6.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

DP
type: SiteQuality
SIO_000300: 1.652913e6

QD
type: SiteQuality
SIO_000300: 1.401e1

MQRankSum
type: SiteQuality
SIO_000300: 8.31e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
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variant carriers: 0

GenotypeQuality
all individuals: 134
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GenotypeQuality
all individuals: 33
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GenotypeQuality
all individuals: 41726
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variant carriers: 0

GenotypeQuality
all individuals: 60
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GenotypeQuality
all individuals: 1666
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GenotypeQuality
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GenotypeQuality
all individuals: 6468
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variant carriers: 0

GenotypeQuality
all individuals: 44
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variant carriers: 0

GenotypeQuality
all individuals: 30
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GenotypeQuality
all individuals: 2667
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 269
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variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64670
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16430
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8322
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9192
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.795074758135444e-5
allele num: 11370
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.4e0

VQSLOD
type: SiteQuality
SIO_000300: 7.39e-1

QD
type: SiteQuality
SIO_000300: 1.404e1

DP
type: SiteQuality
SIO_000300: 1.650163e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 446
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 41
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 76
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1652
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1091
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3661
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40873
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 697
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6393
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2667
bin: 9.75e1
variant carriers: 1

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11302
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16386
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8242
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9118
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.99e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.637714e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.71e1

VQSLOD
type: SiteQuality
SIO_000300: -7.15e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.37e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.854e0

GenotypeQuality
all individuals: 103
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 550
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2718
bin: 9.75e1
variant carriers: 92

GenotypeQuality
all individuals: 136
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 510
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1351
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 574
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38192
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1069
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 689
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 5982
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 85
allele frequency: 9.62409420289855e-3
allele num: 8832
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.18674314850223e-5
allele num: 62760
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6528
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7972
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.508566275924256e-4
allele num: 11090
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16224
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

DP
type: SiteQuality
SIO_000300: 1.596831e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.04e-1

QD
type: SiteQuality
SIO_000300: 1.574e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.95e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.87e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeQuality
all individuals: 2621
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 252
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 890
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1211
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 411
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 756
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 815
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 681
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5033
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32939
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 742
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9004
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 608
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.566416040100251e-4
allele num: 6384
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7490
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59656
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10512
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15838
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8318
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.3e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.79e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.395e0

MQ
type: SiteQuality
SIO_000300: 5.907e1

DP
type: SiteQuality
SIO_000300: 1.507857e6

VQSLOD
type: SiteQuality
SIO_000300: -2.568e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.88e-1

QD
type: SiteQuality
SIO_000300: 1.664e1

GenotypeQuality
all individuals: 11381
bin: 2.25e1
variant carriers: 35

GenotypeQuality
all individuals: 132
bin: 1.25e1
variant carriers: 12

GenotypeQuality
all individuals: 79
bin: 8.75e1
variant carriers: 51

GenotypeQuality
all individuals: 26688
bin: 6.25e1
variant carriers: 64

GenotypeQuality
all individuals: 1353
bin: 7.5e0
variant carriers: 10

GenotypeQuality
all individuals: 296
bin: 2.5e0
variant carriers: 14

GenotypeQuality
all individuals: 406
bin: 3.75e1
variant carriers: 36

GenotypeQuality
all individuals: 12771
bin: 9.75e1
variant carriers: 12639

GenotypeQuality
all individuals: 3170
bin: 6.75e1
variant carriers: 77

GenotypeQuality
all individuals: 685
bin: 3.25e1
variant carriers: 24

GenotypeQuality
all individuals: 535
bin: 7.25e1
variant carriers: 62

GenotypeQuality
all individuals: 213
bin: 4.75e1
variant carriers: 54

GenotypeQuality
all individuals: 207
bin: 8.25e1
variant carriers: 88

GenotypeQuality
all individuals: 122
bin: 9.25e1
variant carriers: 96

GenotypeQuality
all individuals: 246
bin: 1.75e1
variant carriers: 30

GenotypeQuality
all individuals: 330
bin: 5.75e1
variant carriers: 46

GenotypeQuality
all individuals: 348
bin: 5.25e1
variant carriers: 63

African
type: Population
allele count: 192
allele frequency: 2.408429503261415e-2
allele num: 7972
num of homozygotes: 1

Latino
type: Population
allele count: 2749
allele frequency: 2.766150130811028e-1
allele num: 9938
num of homozygotes: 361

East Asian
type: Population
allele count: 822
allele frequency: 1.161673261729791e-1
allele num: 7076
num of homozygotes: 42

European (Non-Finnish)
type: Population
allele count: 7084
allele frequency: 1.240847784200385e-1
allele num: 57090
num of homozygotes: 393

South Asian
type: Population
allele count: 2411
allele frequency: 1.552679031427099e-1
allele num: 15528
num of homozygotes: 208

European (Finnish)
type: Population
allele count: 932
allele frequency: 1.498392282958199e-1
allele num: 6220
num of homozygotes: 71

Other
type: Population
allele count: 138
allele frequency: 1.703703703703704e-1
allele num: 810
num of homozygotes: 8

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.577e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.2e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.4e-2

FS
type: SiteQuality
SIO_000300: 3.009e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.37e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.27e0

DP
type: SiteQuality
SIO_000300: 1.525109e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.579e0

GenotypeQuality
all individuals: 965
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 524
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 551
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1047
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32093
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17415
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2037
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3485
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 752
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5876
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7632
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53272
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.701514542286557e-5
allele num: 14922
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.01e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.3e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.108e0

MQ
type: SiteQuality
SIO_000300: 5.294e1

MQRankSum
type: SiteQuality
SIO_000300: -2.974e0

VQSLOD
type: SiteQuality
SIO_000300: -6.515e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.0e-2

DP
type: SiteQuality
SIO_000300: 1.234065e6

GenotypeQuality
all individuals: 27331
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2024
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1627
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 246
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19121
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 537
bin: 1.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13608
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5306
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.578282828282828e-4
allele num: 6336
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6476
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 636
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4960
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43032
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.11e-2

MQRankSum
type: SiteQuality
SIO_000300: -5.53e-1

MQ
type: SiteQuality
SIO_000300: 5.863e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.0e-2

DP
type: SiteQuality
SIO_000300: 9.53279e5

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.52e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.894e0

QD
type: SiteQuality
SIO_000300: 1.741e1

GenotypeQuality
all individuals: 1844
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1652
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 739
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30685
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 885
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14430
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1522
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 239
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 3.620564808110065e-4
allele num: 5524
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4486
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 564
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12952
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38220
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5732
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.901e1

QD
type: SiteQuality
SIO_000300: 1.511e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.45e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

VQSLOD
type: SiteQuality
SIO_000300: 2.2e0

MQRankSum
type: SiteQuality
SIO_000300: 1.53e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.53e0

DP
type: SiteQuality
SIO_000300: 8.42054e5

ClippingRankSum
type: SiteQuality
SIO_000300: -2.89e-1

GenotypeQuality
all individuals: 394
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1905
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 856
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1664
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11285
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7385
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1216
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 532
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1136
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31489
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 33958
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 498
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4680
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5134
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4160
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12374
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.459419576979833e-4
allele num: 4066
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.48e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.83e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.702e0

DP
type: SiteQuality
SIO_000300: 7.62019e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.379999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.637e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.199999999999999e-2

GenotypeQuality
all individuals: 294
bin: 5.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4980
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4040
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3852
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 4.547521600727603e-4
allele num: 4398
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.070687219799791e-5
allele num: 32566
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.45e0

BaseQRankSum
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SIO_000300: -2.166e0

MQ
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.97e-2

MQRankSum
type: SiteQuality
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DP
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ReadPosRankSum
type: SiteQuality
SIO_000300: 7.76e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.46e-1

QD
type: SiteQuality
SIO_000300: 1.447e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 16

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 460
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3468
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3710
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 4.711583765228512e-4
allele num: 29714
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.162629757785467e-4
allele num: 4624
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3744
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11820
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.25e-2

QD
type: SiteQuality
SIO_000300: 1.411e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 6.89189e5

VQSLOD
type: SiteQuality
SIO_000300: 4.19e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.079e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 64

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3168
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.995805871779509e-4
allele num: 3338
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3508
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4392
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 55
allele frequency: 1.983697612349419e-3
allele num: 27726
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 4.343293954134816e-4
allele num: 11512
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 430
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.0e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.69e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.53e-2

DP
type: SiteQuality
SIO_000300: 6.55543e5

QD
type: SiteQuality
SIO_000300: 1.462e1

MQRankSum
type: SiteQuality
SIO_000300: 2.65e-1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2784
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 3.633720930232558e-4
allele num: 2752
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3116
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 396
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11070
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24642
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4002
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.3e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.62e0

VQSLOD
type: SiteQuality
SIO_000300: -5.499000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.99e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.54e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.54e-1

DP
type: SiteQuality
SIO_000300: 6.06888e5

QD
type: SiteQuality
SIO_000300: 2.027e1

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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variant carriers: 1

South Asian
type: Population
allele count: 1
allele frequency: 9.132420091324201e-5
allele num: 10950
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23728
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2974
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3902
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2596
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.902e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.99e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.15e-2

DP
type: SiteQuality
SIO_000300: 5.98504e5

VQSLOD
type: SiteQuality
SIO_000300: -2.181e0

MQRankSum
type: SiteQuality
SIO_000300: 4.53e-1

QD
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MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.43e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 302
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1538
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2784
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1324
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1870
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 15736
num of homozygotes: 0

VQSLOD
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SIO_000300: -1.823e0

DP
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SIO_000300: 4.80124e5

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 4.21e-1

InbreedingCoeff
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SIO_000300: -4.74e-2

MQ
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BaseQRankSum
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SIO_000300: -2.017e0

MQRankSum
type: SiteQuality
SIO_000300: -4.21e-1

ReadPosRankSum
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SIO_000300: -4.21e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 118
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1192
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1706
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1376
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9238
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 3.831417624521073e-4
allele num: 2610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14666
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 292
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.60968e5

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.92e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.93e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.14e0

MQRankSum
type: SiteQuality
SIO_000300: 1.95e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.84e-1

GenotypeQuality
all individuals: 578
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variant carriers: 48

GenotypeQuality
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GenotypeQuality
all individuals: 240
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GenotypeQuality
all individuals: 133
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GenotypeQuality
all individuals: 482
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GenotypeQuality
all individuals: 103
bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
all individuals: 1515
bin: 1.75e1
variant carriers: 120

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
all individuals: 1472
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 90
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GenotypeQuality
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GenotypeQuality
all individuals: 1707
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variant carriers: 1615

GenotypeQuality
all individuals: 1021
bin: 2.75e1
variant carriers: 78

South Asian
type: Population
allele count: 612
allele frequency: 6.657963446475196e-2
allele num: 9192
num of homozygotes: 29

African
type: Population
allele count: 861
allele frequency: 3.288770053475936e-1
allele num: 2618
num of homozygotes: 123

Latino
type: Population
allele count: 27
allele frequency: 2.327586206896552e-2
allele num: 1160
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 11
allele frequency: 6.618531889290012e-3
allele num: 1662
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 227
allele frequency: 1.586303284416492e-2
allele num: 14310
num of homozygotes: 0

Other
type: Population
allele count: 10
allele frequency: 3.571428571428571e-2
allele num: 280
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1354
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

DP
type: SiteQuality
SIO_000300: 4.57846e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.1e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.61e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.8e1

GenotypeQuality
all individuals: 769
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 199
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18046
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1941
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1118
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3999
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 493
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11714
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 7.668711656441718e-4
allele num: 1304
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8450
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1672
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1040
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

QD
type: SiteQuality
SIO_000300: 1.553e1

VQSLOD
type: SiteQuality
SIO_000300: -2.096e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.67e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.11994e5

ClippingRankSum
type: SiteQuality
SIO_000300: -5.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

MQ
type: SiteQuality
SIO_000300: 5.843e1

GenotypeQuality
all individuals: 58
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1171
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1652
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1076
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11554
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 48
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2395
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 440
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 396
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6064
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 526
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 160
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.26e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

QD
type: SiteQuality
SIO_000300: 2.136e1

DP
type: SiteQuality
SIO_000300: 2.9976e5

VQSLOD
type: SiteQuality
SIO_000300: -1.002e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 30857
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 978
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 857
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7270
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2878
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1193
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 575
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3514
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 494
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 264
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 258
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.992825827022718e-4
allele num: 5018
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.005e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.309999999999999e-2

MQ
type: SiteQuality
SIO_000300: 5.878e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.715e0

VQSLOD
type: SiteQuality
SIO_000300: -5.115e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.16e0

MQRankSum
type: SiteQuality
SIO_000300: -4.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.654e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.20259e5

GenotypeQuality
all individuals: 1194
bin: 1.25e1
variant carriers: 10

GenotypeQuality
all individuals: 38
bin: 4.75e1
variant carriers: 5

GenotypeQuality
all individuals: 29
bin: 9.25e1
variant carriers: 21

GenotypeQuality
all individuals: 28
bin: 8.25e1
variant carriers: 6

GenotypeQuality
all individuals: 185
bin: 9.75e1
variant carriers: 100

GenotypeQuality
all individuals: 610
bin: 2.75e1
variant carriers: 25

GenotypeQuality
all individuals: 6216
bin: 2.25e1
variant carriers: 15

GenotypeQuality
all individuals: 3785
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 8.75e1
variant carriers: 7

GenotypeQuality
all individuals: 28850
bin: 7.5e0
variant carriers: 28

GenotypeQuality
all individuals: 827
bin: 1.75e1
variant carriers: 14

GenotypeQuality
all individuals: 51
bin: 5.25e1
variant carriers: 6

GenotypeQuality
all individuals: 36
bin: 7.25e1
variant carriers: 4

GenotypeQuality
all individuals: 83
bin: 6.75e1
variant carriers: 10

GenotypeQuality
all individuals: 39
bin: 7.75e1
variant carriers: 4

GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 16

GenotypeQuality
all individuals: 558
bin: 6.25e1
variant carriers: 16

South Asian
type: Population
allele count: 4
allele frequency: 8.904719501335708e-4
allele num: 4492
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 4.132231404958678e-3
allele num: 242
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 228
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 7.575757575757576e-3
allele num: 396
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 7.936507936507936e-3
allele num: 126
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 96
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 54
allele frequency: 1.818181818181818e-2
allele num: 2970
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.62e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.3e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.26e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

DP
type: SiteQuality
SIO_000300: 1.97776e5

GenotypeQuality
all individuals: 24
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 838
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 552
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.25e1
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GenotypeQuality
all individuals: 85
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GenotypeQuality
all individuals: 5302
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1528
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variant carriers: 0

GenotypeQuality
all individuals: 51
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variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 3.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 316
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 204
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2188
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 76
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3216
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.6341e5