6-30866961-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30866961
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30866961
    reference: chr 6
allele count: 4
allele frequency: 3.29549012176836e-5
allele num: 121378
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000422442
  ensembl transcript: ENST00000508312
  gene symbol: DDR1
  hgvsc: ENST00000508312.1:c.2573C>T
  hgvsp: ENSP00000422442.1:p.Pro858Leu
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.2519C>T
  hgvsp: ENSP00000406091.2:p.Pro840Leu
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.2519C>T
  hgvsp: ENSP00000365753.3:p.Pro840Leu
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000407699
  ensembl transcript: ENST00000418800
  gene symbol: DDR1
  hgvsc: ENST00000418800.2:c.2519C>T
  hgvsp: ENSP00000407699.2:p.Pro840Leu
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*1687C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.2630C>T
  hgvsp: ENSP00000405039.1:p.Pro877Leu
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-864C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000427552
  ensembl transcript: ENST00000513240
  gene symbol: DDR1
  hgvsc: ENST00000513240.1:c.2648C>T
  hgvsp: ENSP00000427552.1:p.Pro883Leu
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.2630C>T
  hgvsp: ENSP00000365752.3:p.Pro877Leu
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.2648C>T
  hgvsp: ENSP00000365759.3:p.Pro883Leu
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.2519C>T
  hgvsp: ENSP00000365754.4:p.Pro840Leu
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000421978
  ensembl transcript: ENST00000482873
  gene symbol: DDR1
  hgvsc: ENST00000482873.2:c.*1687C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.2630C>T
  hgvsp: ENSP00000318217.8:p.Pro877Leu
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.2519C>T
  hgvsp: ENSP00000365751.2:p.Pro840Leu
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000424003
  ensembl transcript: ENST00000484556
  gene symbol: DDR1
  hgvsc: ENST00000484556.1:c.818C>T
  hgvsp: ENST00000484556.1:c.818C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2205
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5480
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3949
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro883Leu
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD

6-30866962-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30866962
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30866962
    reference: chr 6
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000424003
  ensembl transcript: ENST00000484556
  gene symbol: DDR1
  hgvsc: ENST00000484556.1:c.819G>A
  hgvsp: ENSP00000424003.1:p.Ala274Thr
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.2649G>A
  hgvsp: ENST00000376575.3:c.2649G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.2520G>A
  hgvsp: ENST00000376567.2:c.2520G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*1688G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.2520G>A
  hgvsp: ENST00000376570.4:c.2520G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.2520G>A
  hgvsp: ENST00000454612.2:c.2520G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000422442
  ensembl transcript: ENST00000508312
  gene symbol: DDR1
  hgvsc: ENST00000508312.1:c.2574G>A
  hgvsp: ENST00000508312.1:c.2574G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.2631G>A
  hgvsp: ENST00000376568.3:c.2631G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000421978
  ensembl transcript: ENST00000482873
  gene symbol: DDR1
  hgvsc: ENST00000482873.2:c.*1688G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000427552
  ensembl transcript: ENST00000513240
  gene symbol: DDR1
  hgvsc: ENST00000513240.1:c.2649G>A
  hgvsp: ENST00000513240.1:c.2649G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.2631G>A
  hgvsp: ENST00000324771.8:c.2631G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-863G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.2520G>A
  hgvsp: ENST00000376569.3:c.2520G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000407699
  ensembl transcript: ENST00000418800
  gene symbol: DDR1
  hgvsc: ENST00000418800.2:c.2520G>A
  hgvsp: ENST00000418800.2:c.2520G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.2631G>A
  hgvsp: ENST00000452441.1:c.2631G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2940
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6305
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5475
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6120
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6056
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5697
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2205
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala274Thr
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

6-30866962-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30866962
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30866962
    reference: chr 6
allele count: 4
allele frequency: 3.29549012176836e-5
allele num: 121378
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.2631G>T
  hgvsp: ENST00000376568.3:c.2631G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.2520G>T
  hgvsp: ENST00000376569.3:c.2520G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000424003
  ensembl transcript: ENST00000484556
  gene symbol: DDR1
  hgvsc: ENST00000484556.1:c.819G>T
  hgvsp: ENSP00000424003.1:p.Ala274Ser
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000427552
  ensembl transcript: ENST00000513240
  gene symbol: DDR1
  hgvsc: ENST00000513240.1:c.2649G>T
  hgvsp: ENST00000513240.1:c.2649G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*1688G>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.2520G>T
  hgvsp: ENST00000376570.4:c.2520G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-863G>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000422442
  ensembl transcript: ENST00000508312
  gene symbol: DDR1
  hgvsc: ENST00000508312.1:c.2574G>T
  hgvsp: ENST00000508312.1:c.2574G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.2649G>T
  hgvsp: ENST00000376575.3:c.2649G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.2520G>T
  hgvsp: ENST00000376567.2:c.2520G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.2631G>T
  hgvsp: ENST00000324771.8:c.2631G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.2520G>T
  hgvsp: ENST00000454612.2:c.2520G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.2631G>T
  hgvsp: ENST00000452441.1:c.2631G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000421978
  ensembl transcript: ENST00000482873
  gene symbol: DDR1
  hgvsc: ENST00000482873.2:c.*1688G>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000407699
  ensembl transcript: ENST00000418800
  gene symbol: DDR1
  hgvsc: ENST00000418800.2:c.2520G>T
  hgvsp: ENST00000418800.2:c.2520G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6056
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2940
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3949
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6105
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5475
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala274Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD

6-30866973-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30866973
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30866973
    reference: chr 6
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000422442
  ensembl transcript: ENST00000508312
  gene symbol: DDR1
  hgvsc: ENST00000508312.1:c.2585A>G
  hgvsp: ENSP00000422442.1:p.Tyr862Cys
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.2660A>G
  hgvsp: ENSP00000365759.3:p.Tyr887Cys
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000427552
  ensembl transcript: ENST00000513240
  gene symbol: DDR1
  hgvsc: ENST00000513240.1:c.2660A>G
  hgvsp: ENSP00000427552.1:p.Tyr887Cys
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*1699A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000407699
  ensembl transcript: ENST00000418800
  gene symbol: DDR1
  hgvsc: ENST00000418800.2:c.2531A>G
  hgvsp: ENSP00000407699.2:p.Tyr844Cys
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.2642A>G
  hgvsp: ENSP00000318217.8:p.Tyr881Cys
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.2531A>G
  hgvsp: ENSP00000406091.2:p.Tyr844Cys
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000424003
  ensembl transcript: ENST00000484556
  gene symbol: DDR1
  hgvsc: ENST00000484556.1:c.830A>G
  hgvsp: ENSP00000424003.1:p.Ile277Met
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-852A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000421978
  ensembl transcript: ENST00000482873
  gene symbol: DDR1
  hgvsc: ENST00000482873.2:c.*1699A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.2642A>G
  hgvsp: ENSP00000405039.1:p.Tyr881Cys
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.2642A>G
  hgvsp: ENSP00000365752.3:p.Tyr881Cys
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.2531A>G
  hgvsp: ENSP00000365753.3:p.Tyr844Cys
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.2531A>G
  hgvsp: ENSP00000365754.4:p.Tyr844Cys
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.2531A>G
  hgvsp: ENSP00000365751.2:p.Tyr844Cys
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5486
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5697
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6058
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2205
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr887Cys
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS

6-30866984-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30866984
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30866984
    reference: chr 6
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.2542C>T
  hgvsp: ENSP00000365751.2:p.Leu848Phe
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-841C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000427552
  ensembl transcript: ENST00000513240
  gene symbol: DDR1
  hgvsc: ENST00000513240.1:c.2671C>T
  hgvsp: ENSP00000427552.1:p.Leu891Phe
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.2542C>T
  hgvsp: ENSP00000365753.3:p.Leu848Phe
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.2542C>T
  hgvsp: ENSP00000406091.2:p.Leu848Phe
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000421978
  ensembl transcript: ENST00000482873
  gene symbol: DDR1
  hgvsc: ENST00000482873.2:c.*1710C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*1710C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000407699
  ensembl transcript: ENST00000418800
  gene symbol: DDR1
  hgvsc: ENST00000418800.2:c.2542C>T
  hgvsp: ENSP00000407699.2:p.Leu848Phe
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.2542C>T
  hgvsp: ENSP00000365754.4:p.Leu848Phe
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.2671C>T
  hgvsp: ENSP00000365759.3:p.Leu891Phe
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000422442
  ensembl transcript: ENST00000508312
  gene symbol: DDR1
  hgvsc: ENST00000508312.1:c.2596C>T
  hgvsp: ENSP00000422442.1:p.Leu866Phe
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.2653C>T
  hgvsp: ENSP00000318217.8:p.Leu885Phe
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.2653C>T
  hgvsp: ENSP00000405039.1:p.Leu885Phe
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000424003
  ensembl transcript: ENST00000484556
  gene symbol: DDR1
  hgvsc: ENST00000484556.1:c.*8C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.2653C>T
  hgvsp: ENSP00000365752.3:p.Leu885Phe
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6302
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5472
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3949
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu891Phe
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

6-30866987-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30866987
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30866987
    reference: chr 6
allele count: 4
allele frequency: 3.295761650517435e-5
allele num: 121368
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.2656C>T
  hgvsp: ENSP00000365752.3:p.Arg886Trp
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*1713C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000422442
  ensembl transcript: ENST00000508312
  gene symbol: DDR1
  hgvsc: ENST00000508312.1:c.2599C>T
  hgvsp: ENSP00000422442.1:p.Arg867Trp
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.2545C>T
  hgvsp: ENSP00000365751.2:p.Arg849Trp
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.2545C>T
  hgvsp: ENSP00000365754.4:p.Arg849Trp
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000407699
  ensembl transcript: ENST00000418800
  gene symbol: DDR1
  hgvsc: ENST00000418800.2:c.2545C>T
  hgvsp: ENSP00000407699.2:p.Arg849Trp
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000427552
  ensembl transcript: ENST00000513240
  gene symbol: DDR1
  hgvsc: ENST00000513240.1:c.2674C>T
  hgvsp: ENSP00000427552.1:p.Arg892Trp
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.2545C>T
  hgvsp: ENSP00000365753.3:p.Arg849Trp
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.2656C>T
  hgvsp: ENSP00000405039.1:p.Arg886Trp
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.2656C>T
  hgvsp: ENSP00000318217.8:p.Arg886Trp
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000424003
  ensembl transcript: ENST00000484556
  gene symbol: DDR1
  hgvsc: ENST00000484556.1:c.*11C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-838C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.2545C>T
  hgvsp: ENSP00000406091.2:p.Arg849Trp
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.2674C>T
  hgvsp: ENSP00000365759.3:p.Arg892Trp
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000421978
  ensembl transcript: ENST00000482873
  gene symbol: DDR1
  hgvsc: ENST00000482873.2:c.*1713C>T
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6299
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6106
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6193
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6117
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg892Trp
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

6-30866988-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30866988
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30866988
    reference: chr 6
allele count: 2
allele frequency: 1.647853670594051e-5
allele num: 121370
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-837G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.2657G>A
  hgvsp: ENSP00000405039.1:p.Arg886Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.2546G>A
  hgvsp: ENSP00000406091.2:p.Arg849Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.2546G>A
  hgvsp: ENSP00000365751.2:p.Arg849Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000424003
  ensembl transcript: ENST00000484556
  gene symbol: DDR1
  hgvsc: ENST00000484556.1:c.*12G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.2675G>A
  hgvsp: ENSP00000365759.3:p.Arg892Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.2546G>A
  hgvsp: ENSP00000365754.4:p.Arg849Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*1714G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.2657G>A
  hgvsp: ENSP00000365752.3:p.Arg886Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.2657G>A
  hgvsp: ENSP00000318217.8:p.Arg886Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000407699
  ensembl transcript: ENST00000418800
  gene symbol: DDR1
  hgvsc: ENST00000418800.2:c.2546G>A
  hgvsp: ENSP00000407699.2:p.Arg849Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000422442
  ensembl transcript: ENST00000508312
  gene symbol: DDR1
  hgvsc: ENST00000508312.1:c.2600G>A
  hgvsp: ENSP00000422442.1:p.Arg867Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000421978
  ensembl transcript: ENST00000482873
  gene symbol: DDR1
  hgvsc: ENST00000482873.2:c.*1714G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.2546G>A
  hgvsp: ENSP00000365753.3:p.Arg849Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000427552
  ensembl transcript: ENST00000513240
  gene symbol: DDR1
  hgvsc: ENST00000513240.1:c.2675G>A
  hgvsp: ENSP00000427552.1:p.Arg892Gln
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6070
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6193
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5464
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg892Gln
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum

6-30867000-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867000
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867000
    reference: chr 6
allele count: 2
allele frequency: 1.648505629646725e-5
allele num: 121322
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000427552
  ensembl transcript: ENST00000513240
  gene symbol: DDR1
  hgvsc: ENST00000513240.1:c.2687G>A
  hgvsp: ENSP00000427552.1:p.Arg896Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.2558G>A
  hgvsp: ENSP00000365753.3:p.Arg853Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000424003
  ensembl transcript: ENST00000484556
  gene symbol: DDR1
  hgvsc: ENST00000484556.1:c.*24G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.2669G>A
  hgvsp: ENSP00000405039.1:p.Arg890Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*1726G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.2558G>A
  hgvsp: ENSP00000406091.2:p.Arg853Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.2558G>A
  hgvsp: ENSP00000365754.4:p.Arg853Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.2669G>A
  hgvsp: ENSP00000318217.8:p.Arg890Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.2669G>A
  hgvsp: ENSP00000365752.3:p.Arg890Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000422442
  ensembl transcript: ENST00000508312
  gene symbol: DDR1
  hgvsc: ENST00000508312.1:c.2612G>A
  hgvsp: ENSP00000422442.1:p.Arg871Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.2558G>A
  hgvsp: ENSP00000365751.2:p.Arg853Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000407699
  ensembl transcript: ENST00000418800
  gene symbol: DDR1
  hgvsc: ENST00000418800.2:c.2558G>A
  hgvsp: ENSP00000407699.2:p.Arg853Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.2687G>A
  hgvsp: ENSP00000365759.3:p.Arg896Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-825G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000421978
  ensembl transcript: ENST00000482873
  gene symbol: DDR1
  hgvsc: ENST00000482873.2:c.*1726G>A
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6300
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5694
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6116
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5446
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg896Gln
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

6-30867015-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867015
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867015
    reference: chr 6
allele count: 1
allele frequency: 8.249872126982032e-6
allele num: 121214
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.2573G>A
  hgvsp: ENSP00000406091.2:p.Arg858Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000424003
  ensembl transcript: ENST00000484556
  gene symbol: DDR1
  hgvsc: ENST00000484556.1:c.*39G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000407699
  ensembl transcript: ENST00000418800
  gene symbol: DDR1
  hgvsc: ENST00000418800.2:c.2573G>A
  hgvsp: ENSP00000407699.2:p.Arg858Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*1741G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.2573G>A
  hgvsp: ENSP00000365754.4:p.Arg858Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000422442
  ensembl transcript: ENST00000508312
  gene symbol: DDR1
  hgvsc: ENST00000508312.1:c.2627G>A
  hgvsp: ENSP00000422442.1:p.Arg876Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.2702G>A
  hgvsp: ENSP00000365759.3:p.Arg901Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.2684G>A
  hgvsp: ENSP00000365752.3:p.Arg895Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-810G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000427552
  ensembl transcript: ENST00000513240
  gene symbol: DDR1
  hgvsc: ENST00000513240.1:c.2702G>A
  hgvsp: ENSP00000427552.1:p.Arg901Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.2684G>A
  hgvsp: ENSP00000318217.8:p.Arg895Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.2573G>A
  hgvsp: ENSP00000365753.3:p.Arg858Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.2684G>A
  hgvsp: ENSP00000405039.1:p.Arg895Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000421978
  ensembl transcript: ENST00000482873
  gene symbol: DDR1
  hgvsc: ENST00000482873.2:c.*1741G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.2573G>A
  hgvsp: ENSP00000365751.2:p.Arg858Gln
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5989
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4977
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg901Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
population: African
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff

6-30867030-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867030
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867030
    reference: chr 6
allele count: 1
allele frequency: 8.278693953241936e-6
allele num: 120792
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-795A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.2588A>G
  hgvsp: ENSP00000365751.2:p.Gln863Arg
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000422442
  ensembl transcript: ENST00000508312
  gene symbol: DDR1
  hgvsc: ENST00000508312.1:c.2642A>G
  hgvsp: ENSP00000422442.1:p.Gln881Arg
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.2699A>G
  hgvsp: ENSP00000405039.1:p.Gln900Arg
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000407699
  ensembl transcript: ENST00000418800
  gene symbol: DDR1
  hgvsc: ENST00000418800.2:c.2588A>G
  hgvsp: ENSP00000407699.2:p.Gln863Arg
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.2717A>G
  hgvsp: ENSP00000365759.3:p.Gln906Arg
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.2588A>G
  hgvsp: ENSP00000365753.3:p.Gln863Arg
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.2588A>G
  hgvsp: ENSP00000406091.2:p.Gln863Arg
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.2699A>G
  hgvsp: ENSP00000318217.8:p.Gln900Arg
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*1756A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000424003
  ensembl transcript: ENST00000484556
  gene symbol: DDR1
  hgvsc: ENST00000484556.1:c.*54A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000427552
  ensembl transcript: ENST00000513240
  gene symbol: DDR1
  hgvsc: ENST00000513240.1:c.2717A>G
  hgvsp: ENSP00000427552.1:p.Gln906Arg
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.2699A>G
  hgvsp: ENSP00000365752.3:p.Gln900Arg
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.2588A>G
  hgvsp: ENSP00000365754.4:p.Gln863Arg
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5694
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6186
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4962
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4977
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6296
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5852
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln906Arg
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff

6-30867036-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867036
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867036
    reference: chr 6
allele count: 3
allele frequency: 2.488841693076042e-5
allele num: 120538
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.2594A>G
  hgvsp: ENSP00000365753.3:p.His865Arg
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000407699
  ensembl transcript: ENST00000418800
  gene symbol: DDR1
  hgvsc: ENST00000418800.2:c.2594A>G
  hgvsp: ENSP00000407699.2:p.His865Arg
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.2594A>G
  hgvsp: ENSP00000406091.2:p.His865Arg
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.2594A>G
  hgvsp: ENSP00000365751.2:p.His865Arg
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000422442
  ensembl transcript: ENST00000508312
  gene symbol: DDR1
  hgvsc: ENST00000508312.1:c.2648A>G
  hgvsp: ENSP00000422442.1:p.His883Arg
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.2705A>G
  hgvsp: ENSP00000318217.8:p.His902Arg
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000424003
  ensembl transcript: ENST00000484556
  gene symbol: DDR1
  hgvsc: ENST00000484556.1:c.*60A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000427552
  ensembl transcript: ENST00000513240
  gene symbol: DDR1
  hgvsc: ENST00000513240.1:c.2723A>G
  hgvsp: ENSP00000427552.1:p.His908Arg
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.2705A>G
  hgvsp: ENSP00000365752.3:p.His902Arg
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.2705A>G
  hgvsp: ENSP00000405039.1:p.His902Arg
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.2723A>G
  hgvsp: ENSP00000365759.3:p.His908Arg
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.2594A>G
  hgvsp: ENSP00000365754.4:p.His865Arg
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-789A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*1762A>G
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6183
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5743
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6296
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5694
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6108
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4783
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5994
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His908Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum

6-30867038-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867038
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867038
    reference: chr 6
allele count: 1
allele frequency: 8.308684236764266e-6
allele num: 120356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.2596C>T
  hgvsp: ENSP00000365753.3:p.Arg866Trp
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.2707C>T
  hgvsp: ENSP00000405039.1:p.Arg903Trp
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.2707C>T
  hgvsp: ENSP00000318217.8:p.Arg903Trp
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000422442
  ensembl transcript: ENST00000508312
  gene symbol: DDR1
  hgvsc: ENST00000508312.1:c.2650C>T
  hgvsp: ENSP00000422442.1:p.Arg884Trp
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000424003
  ensembl transcript: ENST00000484556
  gene symbol: DDR1
  hgvsc: ENST00000484556.1:c.*62C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.2725C>T
  hgvsp: ENSP00000365759.3:p.Arg909Trp
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000427552
  ensembl transcript: ENST00000513240
  gene symbol: DDR1
  hgvsc: ENST00000513240.1:c.2725C>T
  hgvsp: ENSP00000427552.1:p.Arg909Trp
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.2596C>T
  hgvsp: ENSP00000406091.2:p.Arg866Trp
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.2707C>T
  hgvsp: ENSP00000365752.3:p.Arg903Trp
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.2596C>T
  hgvsp: ENSP00000365754.4:p.Arg866Trp
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000407699
  ensembl transcript: ENST00000418800
  gene symbol: DDR1
  hgvsc: ENST00000418800.2:c.2596C>T
  hgvsp: ENSP00000407699.2:p.Arg866Trp
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*1764C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.2596C>T
  hgvsp: ENSP00000365751.2:p.Arg866Trp
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-787C>T
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6185
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5994
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3950
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4630
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5695
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg909Trp
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff

6-30867039-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867039
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867039
    reference: chr 6
allele count: 1
allele frequency: 8.30813199960121e-6
allele num: 120364
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.2708G>A
  hgvsp: ENSP00000318217.8:p.Arg903Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000422442
  ensembl transcript: ENST00000508312
  gene symbol: DDR1
  hgvsc: ENST00000508312.1:c.2651G>A
  hgvsp: ENSP00000422442.1:p.Arg884Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.2726G>A
  hgvsp: ENSP00000365759.3:p.Arg909Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.2708G>A
  hgvsp: ENSP00000405039.1:p.Arg903Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.2708G>A
  hgvsp: ENSP00000365752.3:p.Arg903Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.2597G>A
  hgvsp: ENSP00000365751.2:p.Arg866Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.2597G>A
  hgvsp: ENSP00000406091.2:p.Arg866Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000427552
  ensembl transcript: ENST00000513240
  gene symbol: DDR1
  hgvsc: ENST00000513240.1:c.2726G>A
  hgvsp: ENSP00000427552.1:p.Arg909Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000407699
  ensembl transcript: ENST00000418800
  gene symbol: DDR1
  hgvsc: ENST00000418800.2:c.2597G>A
  hgvsp: ENSP00000407699.2:p.Arg866Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.2597G>A
  hgvsp: ENSP00000365754.4:p.Arg866Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000424003
  ensembl transcript: ENST00000484556
  gene symbol: DDR1
  hgvsc: ENST00000484556.1:c.*63G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.2597G>A
  hgvsp: ENSP00000365753.3:p.Arg866Gln
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*1765G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-786G>A
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4975
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5696
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6296
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6180
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg909Gln
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-30867044-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867044
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867044
    reference: chr 6
allele count: 2
allele frequency: 1.665306666222585e-5
allele num: 120098
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.2713C>G
  hgvsp: ENSP00000365752.3:p.Leu905Val
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.2602C>G
  hgvsp: ENSP00000365753.3:p.Leu868Val
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000424003
  ensembl transcript: ENST00000484556
  gene symbol: DDR1
  hgvsc: ENST00000484556.1:c.*68C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-781C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000422442
  ensembl transcript: ENST00000508312
  gene symbol: DDR1
  hgvsc: ENST00000508312.1:c.2656C>G
  hgvsp: ENSP00000422442.1:p.Leu886Val
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.2602C>G
  hgvsp: ENSP00000406091.2:p.Leu868Val
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.2713C>G
  hgvsp: ENSP00000405039.1:p.Leu905Val
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.2731C>G
  hgvsp: ENSP00000365759.3:p.Leu911Val
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.2713C>G
  hgvsp: ENSP00000318217.8:p.Leu905Val
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000407699
  ensembl transcript: ENST00000418800
  gene symbol: DDR1
  hgvsc: ENST00000418800.2:c.2602C>G
  hgvsp: ENSP00000407699.2:p.Leu868Val
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.2602C>G
  hgvsp: ENSP00000365751.2:p.Leu868Val
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.2602C>G
  hgvsp: ENSP00000365754.4:p.Leu868Val
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*1770C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000427552
  ensembl transcript: ENST00000513240
  gene symbol: DDR1
  hgvsc: ENST00000513240.1:c.2731C>G
  hgvsp: ENSP00000427552.1:p.Leu911Val
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3950
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4975
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5527
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6178
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5936
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4391
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu911Val
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

6-30867059-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867059
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867059
    reference: chr 6
allele count: 1
allele frequency: 8.397010664203544e-6
allele num: 119090
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000407699
  ensembl transcript: ENST00000418800
  gene symbol: DDR1
  hgvsc: ENST00000418800.2:c.2617C>G
  hgvsp: ENSP00000407699.2:p.Leu873Val
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.2617C>G
  hgvsp: ENSP00000365754.4:p.Leu873Val
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.2617C>G
  hgvsp: ENSP00000406091.2:p.Leu873Val
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.2728C>G
  hgvsp: ENSP00000318217.8:p.Leu910Val
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.2617C>G
  hgvsp: ENSP00000365753.3:p.Leu873Val
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-766C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000427552
  ensembl transcript: ENST00000513240
  gene symbol: DDR1
  hgvsc: ENST00000513240.1:c.2746C>G
  hgvsp: ENSP00000427552.1:p.Leu916Val
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000422442
  ensembl transcript: ENST00000508312
  gene symbol: DDR1
  hgvsc: ENST00000508312.1:c.2671C>G
  hgvsp: ENSP00000422442.1:p.Leu891Val
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.2728C>G
  hgvsp: ENSP00000365752.3:p.Leu910Val
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.2617C>G
  hgvsp: ENSP00000365751.2:p.Leu873Val
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.2728C>G
  hgvsp: ENSP00000405039.1:p.Leu910Val
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.2746C>G
  hgvsp: ENSP00000365759.3:p.Leu916Val
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000424003
  ensembl transcript: ENST00000484556
  gene symbol: DDR1
  hgvsc: ENST00000484556.1:c.*83C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*1785C>G
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5696
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5034
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6173
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6107
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5855
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu916Val
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD

6-30867061-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867061
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867061
    reference: chr 6
allele count: 2
allele frequency: 1.681407001378754e-5
allele num: 118948
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.2619C>T
  hgvsp: ENST00000376567.2:c.2619C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.2730C>T
  hgvsp: ENST00000376568.3:c.2730C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.2748C>T
  hgvsp: ENST00000376575.3:c.2748C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*1787C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.2619C>T
  hgvsp: ENST00000454612.2:c.2619C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.2619C>T
  hgvsp: ENST00000376569.3:c.2619C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.2730C>T
  hgvsp: ENST00000324771.8:c.2730C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.2619C>T
  hgvsp: ENST00000376570.4:c.2619C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000424003
  ensembl transcript: ENST00000484556
  gene symbol: DDR1
  hgvsc: ENST00000484556.1:c.*85C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.2730C>T
  hgvsp: ENST00000452441.1:c.2730C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000422442
  ensembl transcript: ENST00000508312
  gene symbol: DDR1
  hgvsc: ENST00000508312.1:c.2673C>T
  hgvsp: ENST00000508312.1:c.2673C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-764C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000407699
  ensembl transcript: ENST00000418800
  gene symbol: DDR1
  hgvsc: ENST00000418800.2:c.2619C>T
  hgvsp: ENST00000418800.2:c.2619C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000427552
  ensembl transcript: ENST00000513240
  gene symbol: DDR1
  hgvsc: ENST00000513240.1:c.2748C>T
  hgvsp: ENST00000513240.1:c.2748C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6174
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3288
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4954
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6107
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5848
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu916Leu
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD

6-30867063-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867063
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867063
    reference: chr 6
allele count: 1
allele frequency: 8.412551526878102e-6
allele num: 118870
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000407699
  ensembl transcript: ENST00000418800
  gene symbol: DDR1
  hgvsc: ENST00000418800.2:c.2621A>G
  hgvsp: ENSP00000407699.2:p.Asn874Ser
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.2732A>G
  hgvsp: ENSP00000405039.1:p.Asn911Ser
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000422442
  ensembl transcript: ENST00000508312
  gene symbol: DDR1
  hgvsc: ENST00000508312.1:c.2675A>G
  hgvsp: ENSP00000422442.1:p.Asn892Ser
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.2621A>G
  hgvsp: ENSP00000406091.2:p.Asn874Ser
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.2732A>G
  hgvsp: ENSP00000365752.3:p.Asn911Ser
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.2621A>G
  hgvsp: ENSP00000365753.3:p.Asn874Ser
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000424003
  ensembl transcript: ENST00000484556
  gene symbol: DDR1
  hgvsc: ENST00000484556.1:c.*87A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.2750A>G
  hgvsp: ENSP00000365759.3:p.Asn917Ser
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000427552
  ensembl transcript: ENST00000513240
  gene symbol: DDR1
  hgvsc: ENST00000513240.1:c.2750A>G
  hgvsp: ENSP00000427552.1:p.Asn917Ser
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-762A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.2621A>G
  hgvsp: ENSP00000365751.2:p.Asn874Ser
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.2621A>G
  hgvsp: ENSP00000365754.4:p.Asn874Ser
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.2732A>G
  hgvsp: ENSP00000318217.8:p.Asn911Ser
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*1789A>G
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6294
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6107
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5829
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn917Ser
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum

6-30867064-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867064
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867064
    reference: chr 6
allele count: 1
allele frequency: 8.419351036422112e-6
allele num: 118774
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000427552
  ensembl transcript: ENST00000513240
  gene symbol: DDR1
  hgvsc: ENST00000513240.1:c.2751C>T
  hgvsp: ENST00000513240.1:c.2751C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.2733C>T
  hgvsp: ENST00000452441.1:c.2733C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.2622C>T
  hgvsp: ENST00000454612.2:c.2622C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.2751C>T
  hgvsp: ENST00000376575.3:c.2751C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.2622C>T
  hgvsp: ENST00000376567.2:c.2622C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000407699
  ensembl transcript: ENST00000418800
  gene symbol: DDR1
  hgvsc: ENST00000418800.2:c.2622C>T
  hgvsp: ENST00000418800.2:c.2622C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-761C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.2733C>T
  hgvsp: ENST00000324771.8:c.2733C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*1790C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.2622C>T
  hgvsp: ENST00000376569.3:c.2622C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000422442
  ensembl transcript: ENST00000508312
  gene symbol: DDR1
  hgvsc: ENST00000508312.1:c.2676C>T
  hgvsp: ENST00000508312.1:c.2676C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.2733C>T
  hgvsp: ENST00000376568.3:c.2733C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000424003
  ensembl transcript: ENST00000484556
  gene symbol: DDR1
  hgvsc: ENST00000484556.1:c.*88C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.2622C>T
  hgvsp: ENST00000376570.4:c.2622C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4976
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5697
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6294
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3950
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6107
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn917Asn
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
reference allele: C
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD

6-30867066-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867066
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867066
    reference: chr 6
allele count: 3
allele frequency: 2.530065613034898e-5
allele num: 118574
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.2624C>T
  hgvsp: ENSP00000406091.2:p.Thr875Met
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000427552
  ensembl transcript: ENST00000513240
  gene symbol: DDR1
  hgvsc: ENST00000513240.1:c.2753C>T
  hgvsp: ENSP00000427552.1:p.Thr918Met
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.2624C>T
  hgvsp: ENSP00000365751.2:p.Thr875Met
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.2624C>T
  hgvsp: ENSP00000365754.4:p.Thr875Met
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.2735C>T
  hgvsp: ENSP00000318217.8:p.Thr912Met
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000422442
  ensembl transcript: ENST00000508312
  gene symbol: DDR1
  hgvsc: ENST00000508312.1:c.2678C>T
  hgvsp: ENSP00000422442.1:p.Thr893Met
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.2753C>T
  hgvsp: ENSP00000365759.3:p.Thr918Met
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000424003
  ensembl transcript: ENST00000484556
  gene symbol: DDR1
  hgvsc: ENST00000484556.1:c.*90C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.2624C>T
  hgvsp: ENSP00000365753.3:p.Thr875Met
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000407699
  ensembl transcript: ENST00000418800
  gene symbol: DDR1
  hgvsc: ENST00000418800.2:c.2624C>T
  hgvsp: ENSP00000407699.2:p.Thr875Met
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.2735C>T
  hgvsp: ENSP00000405039.1:p.Thr912Met
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*1792C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.2735C>T
  hgvsp: ENSP00000365752.3:p.Thr912Met
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-759C>T
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5833
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4820
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6174
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6107
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3949
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr918Met
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ

6-30867067-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867067
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867067
    reference: chr 6
allele count: 1
allele frequency: 8.427581789681268e-6
allele num: 118658
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000427552
  ensembl transcript: ENST00000513240
  gene symbol: DDR1
  hgvsc: ENST00000513240.1:c.2754G>A
  hgvsp: ENST00000513240.1:c.2754G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.2625G>A
  hgvsp: ENST00000376569.3:c.2625G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.2625G>A
  hgvsp: ENST00000376570.4:c.2625G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000424003
  ensembl transcript: ENST00000484556
  gene symbol: DDR1
  hgvsc: ENST00000484556.1:c.*91G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.2736G>A
  hgvsp: ENST00000324771.8:c.2736G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.2736G>A
  hgvsp: ENST00000452441.1:c.2736G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000407699
  ensembl transcript: ENST00000418800
  gene symbol: DDR1
  hgvsc: ENST00000418800.2:c.2625G>A
  hgvsp: ENST00000418800.2:c.2625G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000422442
  ensembl transcript: ENST00000508312
  gene symbol: DDR1
  hgvsc: ENST00000508312.1:c.2679G>A
  hgvsp: ENST00000508312.1:c.2679G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.2754G>A
  hgvsp: ENST00000376575.3:c.2754G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.2625G>A
  hgvsp: ENST00000454612.2:c.2625G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.2736G>A
  hgvsp: ENST00000376568.3:c.2736G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*1793G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-758G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.2625G>A
  hgvsp: ENST00000376567.2:c.2625G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3037
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6107
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4815
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4977
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6296
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5698
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr918Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

6-30867075-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867075
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867075
    reference: chr 6
allele count: 1
allele frequency: 8.450513791238508e-6
allele num: 118336
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000407699
  ensembl transcript: ENST00000418800
  gene symbol: DDR1
  hgvsc: ENST00000418800.2:c.*2T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*2T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*1801T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*2T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*2T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000427552
  ensembl transcript: ENST00000513240
  gene symbol: DDR1
  hgvsc: ENST00000513240.1:c.*2T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*2T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*2T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*2T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*2T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-750T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000422442
  ensembl transcript: ENST00000508312
  gene symbol: DDR1
  hgvsc: ENST00000508312.1:c.*2T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*2T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000424003
  ensembl transcript: ENST00000484556
  gene symbol: DDR1
  hgvsc: ENST00000484556.1:c.*99T>C
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5697
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5811
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3949
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4976
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6170
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1358
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2550
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6107
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4672
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP

6-30867080-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867080
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867080
    reference: chr 6
allele count: 1
allele frequency: 8.499065102838687e-6
allele num: 117660
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*7C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-745C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000407699
  ensembl transcript: ENST00000418800
  gene symbol: DDR1
  hgvsc: ENST00000418800.2:c.*7C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*7C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*1806C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000424003
  ensembl transcript: ENST00000484556
  gene symbol: DDR1
  hgvsc: ENST00000484556.1:c.*104C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*7C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*7C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*7C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*7C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*7C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000422442
  ensembl transcript: ENST00000508312
  gene symbol: DDR1
  hgvsc: ENST00000508312.1:c.*7C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*7C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000427552
  ensembl transcript: ENST00000513240
  gene symbol: DDR1
  hgvsc: ENST00000513240.1:c.*7C>T
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4976
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6106
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2258
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5796
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6292
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5698
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6165
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4528
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2691
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD

6-30867082-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867082
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867082
    reference: chr 6
allele count: 1
allele frequency: 8.496609852668785e-6
allele num: 117694
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-743T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*9T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000422442
  ensembl transcript: ENST00000508312
  gene symbol: DDR1
  hgvsc: ENST00000508312.1:c.*9T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*9T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*9T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*9T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*1808T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*9T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*9T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000407699
  ensembl transcript: ENST00000418800
  gene symbol: DDR1
  hgvsc: ENST00000418800.2:c.*9T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*9T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*9T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000424003
  ensembl transcript: ENST00000484556
  gene symbol: DDR1
  hgvsc: ENST00000484556.1:c.*106T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000427552
  ensembl transcript: ENST00000513240
  gene symbol: DDR1
  hgvsc: ENST00000513240.1:c.*9T>C
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4976
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4517
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6290
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6162
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6106
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3949
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/6-30867083-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867083
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867083
    reference: chr 6
allele count: 1
allele frequency: 8.513101663460065e-6
allele num: 117466
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-742C>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*10C>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*10C>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*10C>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000427552
  ensembl transcript: ENST00000513240
  gene symbol: DDR1
  hgvsc: ENST00000513240.1:c.*10C>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*1809C>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*10C>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*10C>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*10C>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000407699
  ensembl transcript: ENST00000418800
  gene symbol: DDR1
  hgvsc: ENST00000418800.2:c.*10C>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000422442
  ensembl transcript: ENST00000508312
  gene symbol: DDR1
  hgvsc: ENST00000508312.1:c.*10C>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000424003
  ensembl transcript: ENST00000484556
  gene symbol: DDR1
  hgvsc: ENST00000484556.1:c.*107C>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*10C>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*10C>A
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1608
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5695
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5782
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6291
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2688
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4977
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6106
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2199
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4487
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP

6-30867083-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867083
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867083
    reference: chr 6
allele count: 3
allele frequency: 2.553930499038019e-5
allele num: 117466
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*10C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*1809C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000422442
  ensembl transcript: ENST00000508312
  gene symbol: DDR1
  hgvsc: ENST00000508312.1:c.*10C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*10C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-742C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000407699
  ensembl transcript: ENST00000418800
  gene symbol: DDR1
  hgvsc: ENST00000418800.2:c.*10C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*10C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*10C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*10C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*10C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000427552
  ensembl transcript: ENST00000513240
  gene symbol: DDR1
  hgvsc: ENST00000513240.1:c.*10C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*10C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000424003
  ensembl transcript: ENST00000484556
  gene symbol: DDR1
  hgvsc: ENST00000484556.1:c.*107C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*10C>G
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2203
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6162
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5695
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1608
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4487
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4977
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6106
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6291
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum

6-30867084-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867084
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867084
    reference: chr 6
allele count: 3
allele frequency: 2.555322737261716e-5
allele num: 117402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*11C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000427552
  ensembl transcript: ENST00000513240
  gene symbol: DDR1
  hgvsc: ENST00000513240.1:c.*11C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*1810C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*11C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000407699
  ensembl transcript: ENST00000418800
  gene symbol: DDR1
  hgvsc: ENST00000418800.2:c.*11C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*11C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*11C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000422442
  ensembl transcript: ENST00000508312
  gene symbol: DDR1
  hgvsc: ENST00000508312.1:c.*11C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*11C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*11C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*11C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000424003
  ensembl transcript: ENST00000484556
  gene symbol: DDR1
  hgvsc: ENST00000484556.1:c.*108C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*11C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-741C>T
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3949
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6106
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6291
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2194
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2203
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5780
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

6-30867086-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867086
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867086
    reference: chr 6
allele count: 1
allele frequency: 8.524422470377632e-6
allele num: 117310
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*13G>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000422442
  ensembl transcript: ENST00000508312
  gene symbol: DDR1
  hgvsc: ENST00000508312.1:c.*13G>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000427552
  ensembl transcript: ENST00000513240
  gene symbol: DDR1
  hgvsc: ENST00000513240.1:c.*13G>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*13G>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*13G>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*13G>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*13G>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-739G>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*1812G>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*13G>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*13G>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000424003
  ensembl transcript: ENST00000484556
  gene symbol: DDR1
  hgvsc: ENST00000484556.1:c.*110G>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*13G>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000407699
  ensembl transcript: ENST00000418800
  gene symbol: DDR1
  hgvsc: ENST00000418800.2:c.*13G>T
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2670
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6289
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3950
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5695
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4978
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1699
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2940
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5788
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4426
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

6-30867087-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867087
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867087
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 116962
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000427552
  ensembl transcript: ENST00000513240
  gene symbol: DDR1
  hgvsc: ENST00000513240.1:c.*14C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*14C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*14C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*1813C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000422442
  ensembl transcript: ENST00000508312
  gene symbol: DDR1
  hgvsc: ENST00000508312.1:c.*14C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*14C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000407699
  ensembl transcript: ENST00000418800
  gene symbol: DDR1
  hgvsc: ENST00000418800.2:c.*14C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*14C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000424003
  ensembl transcript: ENST00000484556
  gene symbol: DDR1
  hgvsc: ENST00000484556.1:c.*111C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*14C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-738C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*14C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*14C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*14C>G
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: 3' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5791
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2085
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5696
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1759
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4402
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6287
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3949
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2629
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

6-30867100-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867100
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867100
    reference: chr 6
allele count: 55
allele frequency: 4.743833017077799e-4
allele num: 115940
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*27A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*27A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000424003
  ensembl transcript: ENST00000484556
  gene symbol: DDR1
  hgvsc: ENST00000484556.1:c.*124A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-725A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*1826A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*27A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000422442
  ensembl transcript: ENST00000508312
  gene symbol: DDR1
  hgvsc: ENST00000508312.1:c.*27A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*27A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*27A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000427552
  ensembl transcript: ENST00000513240
  gene symbol: DDR1
  hgvsc: ENST00000513240.1:c.*27A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000407699
  ensembl transcript: ENST00000418800
  gene symbol: DDR1
  hgvsc: ENST00000418800.2:c.*27A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*27A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*27A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*27A>G
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3947
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2365
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 6101
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5694
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4980
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4304
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6104
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5688
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6274
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2123
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2940
  bin: 6.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
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: A
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ

6-30867104-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867104
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867104
    reference: chr 6
allele count: 3
allele frequency: 2.594976126219639e-5
allele num: 115608
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*1830A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000407699
  ensembl transcript: ENST00000418800
  gene symbol: DDR1
  hgvsc: ENST00000418800.2:c.*31A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*31A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*31A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000422442
  ensembl transcript: ENST00000508312
  gene symbol: DDR1
  hgvsc: ENST00000508312.1:c.*31A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*31A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*31A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*31A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-721A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000424003
  ensembl transcript: ENST00000484556
  gene symbol: DDR1
  hgvsc: ENST00000484556.1:c.*128A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*31A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*31A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*31A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000427552
  ensembl transcript: ENST00000513240
  gene symbol: DDR1
  hgvsc: ENST00000513240.1:c.*31A>G
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2289
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6100
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4252
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2071
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5645
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4982
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3944
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5696
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6274
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

6-30867106-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867106
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867106
    reference: chr 6
allele count: 34086
allele frequency: 2.95926517571885e-1
allele num: 115184
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000424003
  ensembl transcript: ENST00000484556
  gene symbol: DDR1
  hgvsc: ENST00000484556.1:c.*130C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*33C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000407699
  ensembl transcript: ENST00000418800
  gene symbol: DDR1
  hgvsc: ENST00000418800.2:c.*33C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*33C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*33C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*33C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000422442
  ensembl transcript: ENST00000508312
  gene symbol: DDR1
  hgvsc: ENST00000508312.1:c.*33C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*33C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*33C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-719C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*1832C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*33C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*33C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000427552
  ensembl transcript: ENST00000513240
  gene symbol: DDR1
  hgvsc: ENST00000513240.1:c.*33C>T
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5742
  bin: 5.25e1
  variant carriers: 3194
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 9.25e1
  variant carriers: 424
genotype depth: GenotypeDepth
  all individuals: 5453
  bin: 3.25e1
  variant carriers: 829
genotype depth: GenotypeDepth
  all individuals: 6338
  bin: 4.25e1
  variant carriers: 2085
genotype depth: GenotypeDepth
  all individuals: 6222
  bin: 4.75e1
  variant carriers: 2776
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 6.75e1
  variant carriers: 2355
genotype depth: GenotypeDepth
  all individuals: 6063
  bin: 3.75e1
  variant carriers: 1405
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 7.25e1
  variant carriers: 1833
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 1.75e1
  variant carriers: 544
genotype depth: GenotypeDepth
  all individuals: 3812
  bin: 2.75e1
  variant carriers: 527
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 2.5e0
  variant carriers: 75
genotype depth: GenotypeDepth
  all individuals: 5018
  bin: 5.75e1
  variant carriers: 3220
genotype depth: GenotypeDepth
  all individuals: 2283
  bin: 7.5e0
  variant carriers: 1121
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 7.75e1
  variant carriers: 1311
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 1.25e1
  variant carriers: 1300
genotype quality: GenotypeQuality
num of homozygotes: 6373
population: East Asian
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

6-30867107-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867107
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867107
    reference: chr 6
allele count: 2
allele frequency: 1.754324409669836e-5
allele num: 114004
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*34G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-718G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*1833G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000424003
  ensembl transcript: ENST00000484556
  gene symbol: DDR1
  hgvsc: ENST00000484556.1:c.*131G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*34G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000427552
  ensembl transcript: ENST00000513240
  gene symbol: DDR1
  hgvsc: ENST00000513240.1:c.*34G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*34G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*34G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*34G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000422442
  ensembl transcript: ENST00000508312
  gene symbol: DDR1
  hgvsc: ENST00000508312.1:c.*34G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*34G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000407699
  ensembl transcript: ENST00000418800
  gene symbol: DDR1
  hgvsc: ENST00000418800.2:c.*34G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*34G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*34G>A
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: 3' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6060
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2493
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4677
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2036
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8977
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6602
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3156
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

6-30867111-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867111
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867111
    reference: chr 6
allele count: 1
allele frequency: 8.837513477208053e-6
allele num: 113154
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*38C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*38C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*38C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000424003
  ensembl transcript: ENST00000484556
  gene symbol: DDR1
  hgvsc: ENST00000484556.1:c.*135C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*38C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000422442
  ensembl transcript: ENST00000508312
  gene symbol: DDR1
  hgvsc: ENST00000508312.1:c.*38C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000407699
  ensembl transcript: ENST00000418800
  gene symbol: DDR1
  hgvsc: ENST00000418800.2:c.*38C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*38C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-714C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000427552
  ensembl transcript: ENST00000513240
  gene symbol: DDR1
  hgvsc: ENST00000513240.1:c.*38C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*1837C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*38C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*38C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*38C>T
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1840
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1759
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9268
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4675
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5902
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6579
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2726
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

6-30867116-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867116
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867116
    reference: chr 6
allele count: 81
allele frequency: 7.30835859679515e-4
allele num: 110832
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000407699
  ensembl transcript: ENST00000418800
  gene symbol: DDR1
  hgvsc: ENST00000418800.2:c.*43G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*43G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*43G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000424003
  ensembl transcript: ENST00000484556
  gene symbol: DDR1
  hgvsc: ENST00000484556.1:c.*140G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*43G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*43G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*43G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000422442
  ensembl transcript: ENST00000508312
  gene symbol: DDR1
  hgvsc: ENST00000508312.1:c.*43G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000427552
  ensembl transcript: ENST00000513240
  gene symbol: DDR1
  hgvsc: ENST00000513240.1:c.*43G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*43G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*1842G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-709G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*43G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*43G>A
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: 3' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 6.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 6655
  bin: 4.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 3212
  bin: 5.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8412
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2116
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4755
  bin: 5.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

6-30867119-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867119
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867119
    reference: chr 6
allele count: 85
allele frequency: 7.545360934559528e-4
allele num: 112652
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000407699
  ensembl transcript: ENST00000418800
  gene symbol: DDR1
  hgvsc: ENST00000418800.2:c.*46G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000422442
  ensembl transcript: ENST00000508312
  gene symbol: DDR1
  hgvsc: ENST00000508312.1:c.*46G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*46G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*46G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000427552
  ensembl transcript: ENST00000513240
  gene symbol: DDR1
  hgvsc: ENST00000513240.1:c.*46G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*46G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*46G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000424003
  ensembl transcript: ENST00000484556
  gene symbol: DDR1
  hgvsc: ENST00000484556.1:c.*143G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*46G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*46G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*46G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*46G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-706G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*1845G>A
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8205
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8375
  bin: 4.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 6648
  bin: 4.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9143
  bin: 3.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2434
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3224
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3010
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4751
  bin: 5.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum

6-30867780-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867780
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867780
    reference: chr 6
allele count: 1
allele frequency: 8.892999430848037e-6
allele num: 112448
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*707T>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*2506T>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*707T>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*707T>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*707T>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*707T>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-45T>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*707T>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*707T>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*707T>A
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1791
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45801
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1476
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2258
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

6-30867781-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867781
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867781
    reference: chr 6
allele count: 3
allele frequency: 2.667852378835038e-5
allele num: 112450
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*708G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*708G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*708G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*708G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*708G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*2507G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*708G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-44G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*708G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*708G>A
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45801
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2342
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 656
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

6-30867788-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867788
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867788
    reference: chr 6
allele count: 1
allele frequency: 8.891734243846919e-6
allele num: 112464
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*715C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*715C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*715C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-37C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*715C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*715C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*2514C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*715C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*715C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*715C>G
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2281
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45801
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 534
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP

6-30867789-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867789
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867789
    reference: chr 6
allele count: 1
allele frequency: 8.89157612078317e-6
allele num: 112466
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*716C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*2515C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*716C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*716C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*716C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*716C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*716C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*716C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-36C>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*716C>T
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45801
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2337
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3068
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 682
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

6-30867793-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867793
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867793
    reference: chr 6
allele count: 2
allele frequency: 1.777493378837164e-5
allele num: 112518
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*720T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*720T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*2519T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-32T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*720T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*720T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*720T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*720T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*720T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*720T>C
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2534
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45801
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff

6-30867804-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867804
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867804
    reference: chr 6
allele count: 1
allele frequency: 8.881783462119194e-6
allele num: 112590
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*2530A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*731A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*731A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*731A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*731A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*731A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*731A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*731A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*731A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-21A>G
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45801
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2893
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

6-30867816-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867816
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867816
    reference: chr 6
allele count: 2
allele frequency: 1.775410563692854e-5
allele num: 112650
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1292-9G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*2542G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*743G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*743G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*743G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*743G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*743G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*743G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*743G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*743G>A
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45801
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3028
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: ReadPosRankSum

6-30867827-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867827
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867827
    reference: chr 6
allele count: 1
allele frequency: 8.873744365172327e-6
allele num: 112692
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*754T>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1294T>A
  hgvsp: ENSP00000354844.4:p.Phe432Ile
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*754T>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*754T>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*754T>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*754T>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*754T>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*754T>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*2553T>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*754T>A
  variant of: http://identifiers.org/hgnc/2730
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45801
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2958
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Phe432Ile
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP

6-30867830-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867830
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867830
    reference: chr 6
allele count: 1684
allele frequency: 1.4943650723223e-2
allele num: 112690
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*757T>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*757T>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*757T>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*757T>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*757T>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*757T>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*757T>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*757T>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*2556T>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1297T>G
  hgvsp: ENSP00000354844.4:p.Trp433Gly
  variant of: http://identifiers.org/hgnc/2730
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 2.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 45884
  bin: 9.75e1
  variant carriers: 1420
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 3.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 2.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 4.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 3.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2911
  bin: 2.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.75e1
  variant carriers: 1
hgvs: p.Trp433Gly
num of homozygotes: 28
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

6-30867831-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867831
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867831
    reference: chr 6
allele count: 2
allele frequency: 1.774906373688788e-5
allele num: 112682
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*758G>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*758G>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*758G>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*758G>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*758G>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*2557G>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*758G>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1298G>T
  hgvsp: ENSP00000354844.4:p.Trp433Leu
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*758G>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*758G>T
  variant of: http://identifiers.org/hgnc/2730
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2005
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45750
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Trp433Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff

6-30867835-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867835
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867835
    reference: chr 6
allele count: 140
allele frequency: 1.242346259650368e-3
allele num: 112690
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*762G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*762G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*2561G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1302G>A
  hgvsp: ENST00000361741.4:c.1302G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*762G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*762G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*762G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*762G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*762G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*762G>A
  variant of: http://identifiers.org/hgnc/2730
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 4.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45758
  bin: 9.75e1
  variant carriers: 64
genotype depth: GenotypeDepth
  all individuals: 2002
  bin: 2.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 3.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly434Gly
num of homozygotes: 1
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

6-30867837-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867837
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867837
    reference: chr 6
allele count: 3
allele frequency: 2.662076064386746e-5
allele num: 112694
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*764A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1304A>G
  hgvsp: ENSP00000354844.4:p.Glu435Gly
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*2563A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*764A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*764A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*764A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*764A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*764A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*764A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*764A>G
  variant of: http://identifiers.org/hgnc/2730
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2889
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2027
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45748
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 762
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Glu435Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

6-30867838-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867838
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867838
    reference: chr 6
allele count: 1
allele frequency: 8.87342940299567e-6
allele num: 112696
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*765G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1305G>A
  hgvsp: ENST00000361741.4:c.1305G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*765G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*765G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*2564G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*765G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*765G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*765G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*765G>A
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*765G>A
  variant of: http://identifiers.org/hgnc/2730
canonical: false
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45748
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2893
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2030
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Glu435Glu
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

6-30867839-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867839
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867839
    reference: chr 6
allele count: 1
allele frequency: 8.87342940299567e-6
allele num: 112696
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*766A>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*766A>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*766A>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*766A>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*766A>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*766A>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*766A>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*766A>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1306A>T
  hgvsp: ENSP00000354844.4:p.Arg436Ter
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*2565A>T
  variant of: http://identifiers.org/hgnc/2730
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2891
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45748
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 552
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg436Ter
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

6-30867840-GAC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867840
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867838
    reference: chr 6
allele count: 15
allele frequency: 1.330990789543736e-4
allele num: 112698
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*771_*772delCA
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*771_*772delCA
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*771_*772delCA
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*771_*772delCA
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*771_*772delCA
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*2570_*2571delCA
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*771_*772delCA
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*771_*772delCA
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1311_1312delCA
  hgvsp: ENSP00000354844.4:p.His437GlnfsTer15
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*771_*772delCA
  variant of: http://identifiers.org/hgnc/2730
canonical: false
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2890
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2038
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45749
  bin: 9.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 2.25e1
  variant carriers: 0
hgvs: p.His437GlnfsTer15
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: GAC
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

6-30867842-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867842
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867842
    reference: chr 6
allele count: 3
allele frequency: 2.662076064386746e-5
allele num: 112694
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*769C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*769C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*769C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*2568C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*769C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*769C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*769C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*769C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1309C>G
  hgvsp: ENSP00000354844.4:p.His437Asp
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*769C>G
  variant of: http://identifiers.org/hgnc/2730
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2044
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2890
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45746
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 763
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
hgvs: p.His437Asp
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

6-30867847-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867847
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867846
    reference: chr 6
allele count: 3
allele frequency: 2.661934338952973e-5
allele num: 112700
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*779delT
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*2578delT
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*779delT
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*779delT
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*779delT
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*779delT
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.1319delT
  hgvsp: ENSP00000354844.4:p.Leu440TyrfsTer7
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*779delT
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*779delT
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*779delT
  variant of: http://identifiers.org/hgnc/2730
canonical: false
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45746
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50391
  bin: 9.75e1
  variant carriers: 3
hgvs: p.Leu440TyrfsTer7
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
reference allele: AT
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

6-30867862-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867862
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867862
    reference: chr 6
allele count: 1
allele frequency: 8.875477056891809e-6
allele num: 112670
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*789T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*789T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*2588T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*789T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*789T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*789T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*789T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*789T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*789T>C
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.*3T>C
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2064
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45746
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

6-30867869-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867869
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867869
    reference: chr 6
allele count: 14
allele frequency: 1.242632961726905e-4
allele num: 112664
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*796C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*796C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*796C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*2595C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*796C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*796C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*796C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*796C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*796C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.*10C>G
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45748
  bin: 9.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2059
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2725
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50392
  bin: 9.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: African
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-30867882-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867882
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867882
    reference: chr 6
allele count: 3
allele frequency: 2.663777947470299e-5
allele num: 112622
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*809A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*809A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*809A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*809A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*2608A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*809A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.*23A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*809A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*809A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*809A>G
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2371
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45745
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

6-30867890-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867890
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867890
    reference: chr 6
allele count: 3
allele frequency: 2.66519784652014e-5
allele num: 112562
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*817C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*2616C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*817C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*817C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.*31C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*817C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*817C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*817C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*817C>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*817C>G
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45745
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD

6-30867904-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867904
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867904
    reference: chr 6
allele count: 1
allele frequency: 8.892683100345036e-6
allele num: 112452
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*831A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.*45A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*831A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*831A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*831A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*2630A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*831A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*831A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*831A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*831A>G
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45744
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum

6-30867905-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867905
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867905
    reference: chr 6
allele count: 1
allele frequency: 8.892841262783459e-6
allele num: 112450
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*832G>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*832G>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*832G>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*832G>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*832G>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*832G>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*2631G>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.*46G>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*832G>T
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*832G>T
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1822
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45744
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50392
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 603
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 397
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP

6-30867908-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867908
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867908
    reference: chr 6
allele count: 1
allele frequency: 8.895530885283234e-6
allele num: 112416
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*835A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*835A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*835A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.*49A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*835A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*835A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*835A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*835A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*835A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*2634A>G
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45744
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 528
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 816
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

6-30867909-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30867909
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30867909
    reference: chr 6
allele count: 1
allele frequency: 8.896480552293512e-6
allele num: 112404
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365759
  ensembl transcript: ENST00000376575
  gene symbol: DDR1
  hgvsc: ENST00000376575.3:c.*836A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000354844
  ensembl transcript: ENST00000361741
  gene symbol: DDR1
  hgvsc: ENST00000361741.4:c.*50A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000406091
  ensembl transcript: ENST00000454612
  gene symbol: DDR1
  hgvsc: ENST00000454612.2:c.*836A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365754
  ensembl transcript: ENST00000376570
  gene symbol: DDR1
  hgvsc: ENST00000376570.4:c.*836A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365753
  ensembl transcript: ENST00000376569
  gene symbol: DDR1
  hgvsc: ENST00000376569.3:c.*836A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000318217
  ensembl transcript: ENST00000324771
  gene symbol: DDR1
  hgvsc: ENST00000324771.8:c.*836A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405998
  ensembl transcript: ENST00000446312
  gene symbol: DDR1
  hgvsc: ENST00000446312.1:c.*2635A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365752
  ensembl transcript: ENST00000376568
  gene symbol: DDR1
  hgvsc: ENST00000376568.3:c.*836A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000405039
  ensembl transcript: ENST00000452441
  gene symbol: DDR1
  hgvsc: ENST00000452441.1:c.*836A>G
  variant of: http://identifiers.org/hgnc/2730
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000204580
  ensembl protein: ENSP00000365751
  ensembl transcript: ENST00000376567
  gene symbol: DDR1
  hgvsc: ENST00000376567.2:c.*836A>G
  variant of: http://identifiers.org/hgnc/2730
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45744
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 559
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 567
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

6-30876767-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30876767
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30876767
    reference: chr 6
allele count: 1
allele frequency: 8.274857672448034e-6
allele num: 120848
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213780
  ensembl protein: ENSP00000259895
  ensembl transcript: ENST00000259895
  gene symbol: GTF2H4
  hgvsc: ENST00000259895.4:c.-3-44G>A
  variant of: http://identifiers.org/hgnc/4658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213780
  ensembl protein: ENSP00000442700
  ensembl transcript: ENST00000539324
  gene symbol: GTF2H4
  hgvsc: ENST00000539324.1:c.-31-445G>A
  variant of: http://identifiers.org/hgnc/4658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213780
  ensembl protein: ENSP00000410160
  ensembl transcript: ENST00000453897
  gene symbol: GTF2H4
  hgvsc: ENST00000453897.2:c.-3-44G>A
  variant of: http://identifiers.org/hgnc/4658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213780
  ensembl protein: ENSP00000365493
  ensembl transcript: ENST00000376316
  gene symbol: GTF2H4
  hgvsc: ENST00000376316.2:c.-3-44G>A
  variant of: http://identifiers.org/hgnc/4658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137411
  ensembl transcript: ENST00000477288
  gene symbol: VARS2
  hgvsc: ENST00000477288.1:n.163-44G>A
  variant of: http://identifiers.org/hgnc/21642
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10025
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31622
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14235
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2458
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1560
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 42093
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD

6-30876773-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30876773
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30876773
    reference: chr 6
allele count: 1
allele frequency: 8.274309922552459e-6
allele num: 120856
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213780
  ensembl protein: ENSP00000365493
  ensembl transcript: ENST00000376316
  gene symbol: GTF2H4
  hgvsc: ENST00000376316.2:c.-3-38G>C
  variant of: http://identifiers.org/hgnc/4658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213780
  ensembl protein: ENSP00000442700
  ensembl transcript: ENST00000539324
  gene symbol: GTF2H4
  hgvsc: ENST00000539324.1:c.-31-439G>C
  variant of: http://identifiers.org/hgnc/4658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213780
  ensembl protein: ENSP00000410160
  ensembl transcript: ENST00000453897
  gene symbol: GTF2H4
  hgvsc: ENST00000453897.2:c.-3-38G>C
  variant of: http://identifiers.org/hgnc/4658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213780
  ensembl protein: ENSP00000259895
  ensembl transcript: ENST00000259895
  gene symbol: GTF2H4
  hgvsc: ENST00000259895.4:c.-3-38G>C
  variant of: http://identifiers.org/hgnc/4658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137411
  ensembl transcript: ENST00000477288
  gene symbol: VARS2
  hgvsc: ENST00000477288.1:n.163-38G>C
  variant of: http://identifiers.org/hgnc/21642
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14352
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10020
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31645
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42406
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1548
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2441
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1143
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2586
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

6-30876776-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30876776
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30876776
    reference: chr 6
allele count: 117
allele frequency: 9.681102818276598e-4
allele num: 120854
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137411
  ensembl transcript: ENST00000477288
  gene symbol: VARS2
  hgvsc: ENST00000477288.1:n.163-35G>A
  variant of: http://identifiers.org/hgnc/21642
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213780
  ensembl protein: ENSP00000365493
  ensembl transcript: ENST00000376316
  gene symbol: GTF2H4
  hgvsc: ENST00000376316.2:c.-3-35G>A
  variant of: http://identifiers.org/hgnc/4658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213780
  ensembl protein: ENSP00000410160
  ensembl transcript: ENST00000453897
  gene symbol: GTF2H4
  hgvsc: ENST00000453897.2:c.-3-35G>A
  variant of: http://identifiers.org/hgnc/4658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213780
  ensembl protein: ENSP00000259895
  ensembl transcript: ENST00000259895
  gene symbol: GTF2H4
  hgvsc: ENST00000259895.4:c.-3-35G>A
  variant of: http://identifiers.org/hgnc/4658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213780
  ensembl protein: ENSP00000442700
  ensembl transcript: ENST00000539324
  gene symbol: GTF2H4
  hgvsc: ENST00000539324.1:c.-31-436G>A
  variant of: http://identifiers.org/hgnc/4658
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10022
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 4.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 14404
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1780
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 31648
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 4.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2574
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2434
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42502
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1570
  bin: 9.75e1
  variant carriers: 116
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/6-30876794-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30876794
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30876794
    reference: chr 6
allele count: 2
allele frequency: 1.653739932858159e-5
allele num: 120938
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213780
  ensembl protein: ENSP00000442700
  ensembl transcript: ENST00000539324
  gene symbol: GTF2H4
  hgvsc: ENST00000539324.1:c.-31-418A>C
  variant of: http://identifiers.org/hgnc/4658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213780
  ensembl protein: ENSP00000259895
  ensembl transcript: ENST00000259895
  gene symbol: GTF2H4
  hgvsc: ENST00000259895.4:c.-3-17A>C
  variant of: http://identifiers.org/hgnc/4658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213780
  ensembl protein: ENSP00000365493
  ensembl transcript: ENST00000376316
  gene symbol: GTF2H4
  hgvsc: ENST00000376316.2:c.-3-17A>C
  variant of: http://identifiers.org/hgnc/4658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213780
  ensembl protein: ENSP00000410160
  ensembl transcript: ENST00000453897
  gene symbol: GTF2H4
  hgvsc: ENST00000453897.2:c.-3-17A>C
  variant of: http://identifiers.org/hgnc/4658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137411
  ensembl transcript: ENST00000477288
  gene symbol: VARS2
  hgvsc: ENST00000477288.1:n.163-17A>C
  variant of: http://identifiers.org/hgnc/21642
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14627
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10017
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31793
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 406
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42873
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2429
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1134
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8788
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS

6-30876795-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30876795
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30876795
    reference: chr 6
allele count: 2
allele frequency: 1.653739932858159e-5
allele num: 120938
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213780
  ensembl protein: ENSP00000442700
  ensembl transcript: ENST00000539324
  gene symbol: GTF2H4
  hgvsc: ENST00000539324.1:c.-31-417C>G
  variant of: http://identifiers.org/hgnc/4658
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000213780
  ensembl protein: ENSP00000259895
  ensembl transcript: ENST00000259895
  gene symbol: GTF2H4
  hgvsc: ENST00000259895.4:c.-3-16C>G
  variant of: http://identifiers.org/hgnc/4658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137411
  ensembl transcript: ENST00000477288
  gene symbol: VARS2
  hgvsc: ENST00000477288.1:n.163-16C>G
  variant of: http://identifiers.org/hgnc/21642
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213780
  ensembl protein: ENSP00000410160
  ensembl transcript: ENST00000453897
  gene symbol: GTF2H4
  hgvsc: ENST00000453897.2:c.-3-16C>G
  variant of: http://identifiers.org/hgnc/4658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213780
  ensembl protein: ENSP00000365493
  ensembl transcript: ENST00000376316
  gene symbol: GTF2H4
  hgvsc: ENST00000376316.2:c.-3-16C>G
  variant of: http://identifiers.org/hgnc/4658
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10021
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31794
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14627
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2579
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 405
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2429
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8791
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: DP

6-30876811-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30876811
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30876811
    reference: chr 6
allele count: 1
allele frequency: 8.263370132874991e-6
allele num: 121016
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000213780
  ensembl protein: ENSP00000365493
  ensembl transcript: ENST00000376316
  gene symbol: GTF2H4
  hgvsc: ENST00000376316.2:c.-3G>C
  variant of: http://identifiers.org/hgnc/4658
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000213780
  ensembl protein: ENSP00000259895
  ensembl transcript: ENST00000259895
  gene symbol: GTF2H4
  hgvsc: ENST00000259895.4:c.-3G>C
  variant of: http://identifiers.org/hgnc/4658
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000213780
  ensembl protein: ENSP00000410160
  ensembl transcript: ENST00000453897
  gene symbol: GTF2H4
  hgvsc: ENST00000453897.2:c.-3G>C
  variant of: http://identifiers.org/hgnc/4658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213780
  ensembl protein: ENSP00000442700
  ensembl transcript: ENST00000539324
  gene symbol: GTF2H4
  hgvsc: ENST00000539324.1:c.-31-401G>C
  variant of: http://identifiers.org/hgnc/4658
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137411
  ensembl transcript: ENST00000477288
  gene symbol: VARS2
  hgvsc: ENST00000477288.1:n.163G>C
  variant of: http://identifiers.org/hgnc/21642
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31865
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14712
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10014
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1763
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8809
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2572
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1130
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43019
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2436
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 9.25e1
  variant carriers: 0
hgvs: c.-3G>C
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum

6-30876812-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30876812
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 30876812
    reference: chr 6
allele count: 1
allele frequency: 8.263233568560049e-6
allele num: 121018
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137411
  ensembl transcript: ENST00000477288
  gene symbol: VARS2
  hgvsc: ENST00000477288.1:n.164T>C
  variant of: http://identifiers.org/hgnc/21642
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000213780
  ensembl protein: ENSP00000410160
  ensembl transcript: ENST00000453897
  gene symbol: GTF2H4
  hgvsc: ENST00000453897.2:c.-2T>C
  variant of: http://identifiers.org/hgnc/4658
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000213780
  ensembl protein: ENSP00000365493
  ensembl transcript: ENST00000376316
  gene symbol: GTF2H4
  hgvsc: ENST00000376316.2:c.-2T>C
  variant of: http://identifiers.org/hgnc/4658
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000213780
  ensembl protein: ENSP00000259895
  ensembl transcript: ENST00000259895
  gene symbol: GTF2H4
  hgvsc: ENST00000259895.4:c.-2T>C
  variant of: http://identifiers.org/hgnc/4658
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000213780
  ensembl protein: ENSP00000442700
  ensembl transcript: ENST00000539324
  gene symbol: GTF2H4
  hgvsc: ENST00000539324.1:c.-31-400T>C
  variant of: http://identifiers.org/hgnc/4658
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10016
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1764
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31872
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14706
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1131
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2572
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1437
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 42999
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8807
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 9.25e1
  variant carriers: 0
hgvs: c.-2T>C
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

GenotypeDepth
all individuals: 6114
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5697
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 897
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 6303
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4978
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 710
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1529
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 6057
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6105
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 6190
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2986
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3570
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11110
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1727
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33556
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 2940
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1664
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3048
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66710
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: 908
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.422480620155039e-4
allele num: 16512
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e0

MQ
type: SiteQuality
SIO_000300: 5.955e1

MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.48e0

DP
type: SiteQuality
SIO_000300: 2.845072e6

FS
type: SiteQuality
SIO_000300: 4.448e0

QD
type: SiteQuality
SIO_000300: 1.204e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 9.6e-1

GenotypeDepth
all individuals: 1031
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4977
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6190
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1528
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 449
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3949
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 709
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6105
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1665
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2985
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1728
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3048
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11111
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3573
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2940
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33553
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 33
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66710
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.66e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.13e-1

FS
type: SiteQuality
SIO_000300: 5.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.17e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.55e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.07e0

DP
type: SiteQuality
SIO_000300: 2.845422e6

QD
type: SiteQuality
SIO_000300: 1.14e1

GenotypeDepth
all individuals: 1528
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4977
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6190
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1031
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6120
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2205
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5697
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 899
bin: 9.75e1
variant carriers: 4

GenotypeDepth
all individuals: 6305
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11111
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3573
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1728
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1665
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3048
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2985
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33553
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 2940
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.99610253335332e-5
allele num: 66710
num of homozygotes: 0

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

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.845422e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.07e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.13e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.66e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.17e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

FS
type: SiteQuality
SIO_000300: 5.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.55e-1

QD
type: SiteQuality
SIO_000300: 1.14e1

GenotypeDepth
all individuals: 1528
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4977
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6191
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3949
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6303
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 709
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6105
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1031
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6122
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 449
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2941
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11144
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.25e1
variant carriers: 0

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

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

European (Non-Finnish)
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European (Finnish)
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East Asian
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African
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Other
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Latino
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MQRankSum
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DP
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SIO_000300: 2.844887e6

MQ
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QD
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VQSLOD
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ReadPosRankSum
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FS
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SIO_000300: 5.064e0

ClippingRankSum
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InbreedingCoeff
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SIO_000300: -1.0e-4

BaseQRankSum
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SIO_000300: 2.12e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

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

Latino
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Other
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European (Non-Finnish)
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East Asian
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African
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South Asian
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FS
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MQ
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DP
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QD
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BaseQRankSum
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VQSLOD
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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East Asian
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Other
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Latino
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African
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MQRankSum
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FS
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BaseQRankSum
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MQ
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ReadPosRankSum
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ClippingRankSum
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DP
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VQSLOD
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QD
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Non-Finnish)
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Latino
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South Asian
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European (Finnish)
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Other
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FS
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DP
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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MQ
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QD
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VQSLOD
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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East Asian
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Other
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Latino
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South Asian
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DP
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VQSLOD
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MQ
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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QD
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FS
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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European (Non-Finnish)
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allele num: 66446
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Other
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Latino
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European (Finnish)
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East Asian
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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FS
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VQSLOD
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MQRankSum
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QD
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MQ
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DP
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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num of homozygotes: 0

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

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

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

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

Other
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 66046
num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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allele num: 10364
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Latino
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European (Non-Finnish)
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allele num: 65976
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Other
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European (Finnish)
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East Asian
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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FS
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DP
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VQSLOD
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QD
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MQRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

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

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

African
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European (Non-Finnish)
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allele num: 65672
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South Asian
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European (Finnish)
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Other
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East Asian
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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FS
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QD
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DP
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ReadPosRankSum
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MQ
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MQRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele num: 65654
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Other
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European (Finnish)
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African
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Latino
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South Asian
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East Asian
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MQRankSum
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InbreedingCoeff
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MQ
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FS
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QD
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DP
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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African
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European (Non-Finnish)
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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QD
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MQ
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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European (Finnish)
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South Asian
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DP
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ReadPosRankSum
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FS
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QD
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MQRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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BaseQRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1567
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1716
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3076
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2889
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 662
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 3040
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 653
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5766
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33553
bin: 9.75e1
variant carriers: 60

GenotypeQuality
all individuals: 599
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2902
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2733
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 3
allele frequency: 2.598752598752599e-4
allele num: 11544
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.317497103128621e-4
allele num: 8630
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 43
allele frequency: 6.592463128200411e-4
allele num: 65226
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 5.491057420771886e-4
allele num: 12748
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10336
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -4.8e-2

QD
type: SiteQuality
SIO_000300: 1.572e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.28e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.04e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.79e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.65e-1

DP
type: SiteQuality
SIO_000300: 2.760802e6

MQ
type: SiteQuality
SIO_000300: 5.971e1

GenotypeDepth
all individuals: 450
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6089
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1029
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2936
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2200
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5496
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2894
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2889
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1560
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3043
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2443
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 704
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 633
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 580
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3026
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33532
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1716
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 706
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10330
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65158
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.475440222428174e-4
allele num: 8632
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12496
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.860000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.4e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.54e-1

MQ
type: SiteQuality
SIO_000300: 5.953e1

FS
type: SiteQuality
SIO_000300: 1.75e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 4.4e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.3e-2

DP
type: SiteQuality
SIO_000300: 2.757857e6

QD
type: SiteQuality
SIO_000300: 1.351e1

GenotypeDepth
all individuals: 751
bin: 8.75e1
variant carriers: 682

GenotypeDepth
all individuals: 1114
bin: 8.25e1
variant carriers: 961

GenotypeDepth
all individuals: 1636
bin: 2.25e1
variant carriers: 344

GenotypeDepth
all individuals: 4060
bin: 6.25e1
variant carriers: 2926

GenotypeDepth
all individuals: 1109
bin: 9.75e1
variant carriers: 1023

GenotypeQuality
all individuals: 2460
bin: 6.75e1
variant carriers: 89

GenotypeQuality
all individuals: 381
bin: 3.75e1
variant carriers: 188

GenotypeQuality
all individuals: 2136
bin: 9.25e1
variant carriers: 123

GenotypeQuality
all individuals: 39558
bin: 9.75e1
variant carriers: 26625

GenotypeQuality
all individuals: 356
bin: 2.75e1
variant carriers: 109

GenotypeQuality
all individuals: 141
bin: 5.75e1
variant carriers: 75

GenotypeQuality
all individuals: 4245
bin: 6.25e1
variant carriers: 67

GenotypeQuality
all individuals: 211
bin: 4.25e1
variant carriers: 116

GenotypeQuality
all individuals: 2347
bin: 7.75e1
variant carriers: 185

GenotypeQuality
all individuals: 179
bin: 5.25e1
variant carriers: 109

GenotypeQuality
all individuals: 248
bin: 4.75e1
variant carriers: 140

GenotypeQuality
all individuals: 389
bin: 2.5e0
variant carriers: 8

GenotypeQuality
all individuals: 1311
bin: 7.25e1
variant carriers: 117

GenotypeQuality
all individuals: 513
bin: 7.5e0
variant carriers: 44

GenotypeQuality
all individuals: 2338
bin: 8.25e1
variant carriers: 207

GenotypeQuality
all individuals: 1411
bin: 2.25e1
variant carriers: 193

GenotypeQuality
all individuals: 501
bin: 3.25e1
variant carriers: 197

GenotypeQuality
all individuals: 1331
bin: 8.75e1
variant carriers: 136

GenotypeQuality
all individuals: 292
bin: 1.75e1
variant carriers: 146

GenotypeQuality
all individuals: 253
bin: 1.25e1
variant carriers: 61

East Asian
type: Population
allele count: 4957
allele frequency: 5.767977658831743e-1
allele num: 8594
num of homozygotes: 1429

Other
type: Population
allele count: 223
allele frequency: 2.667464114832536e-1
allele num: 836
num of homozygotes: 26

Latino
type: Population
allele count: 5647
allele frequency: 4.908727399165508e-1
allele num: 11504
num of homozygotes: 1461

South Asian
type: Population
allele count: 6216
allele frequency: 5.040544923775543e-1
allele num: 12332
num of homozygotes: 1614

African
type: Population
allele count: 2779
allele frequency: 2.69387359441644e-1
allele num: 10316
num of homozygotes: 368

European (Non-Finnish)
type: Population
allele count: 12590
allele frequency: 1.936625134594678e-1
allele num: 65010
num of homozygotes: 1245

European (Finnish)
type: Population
allele count: 1674
allele frequency: 2.539441747572815e-1
allele num: 6592
num of homozygotes: 230

BaseQRankSum
type: SiteQuality
SIO_000300: 2.54e0

QD
type: SiteQuality
SIO_000300: 1.826e1

DP
type: SiteQuality
SIO_000300: 2.803306e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.32e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.085e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.68e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.52e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

GenotypeDepth
all individuals: 1273
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 8396
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 99
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 254
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9376
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 426
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4238
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7050
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2783
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2333
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 512
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 516
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4460
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 637
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1159
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 24822
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2347
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4234
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4138
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.544115376300917e-5
allele num: 64762
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 8.776549060909251e-5
allele num: 11394
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10298
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.491e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.198e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.73e-1

MQ
type: SiteQuality
SIO_000300: 5.958e1

QD
type: SiteQuality
SIO_000300: 3.202e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -5.0e-1

DP
type: SiteQuality
SIO_000300: 2.355184e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.41e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.987e0

GenotypeDepth
all individuals: 2036
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 164
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8789
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8354
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3154
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1269
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 511
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24815
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 617
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2252
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4127
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 701
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 674
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2235
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 687
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4101
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 495
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4046
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4182
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6354
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2319
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64508
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.165501165501166e-4
allele num: 8580
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10854
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10276
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.0e-1

QD
type: SiteQuality
SIO_000300: 2.259e1

DP
type: SiteQuality
SIO_000300: 2.343972e6

MQRankSum
type: SiteQuality
SIO_000300: -1.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 2.163e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.724e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.01e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.31e-1

GenotypeDepth
all individuals: 1316
bin: 6.75e1
variant carriers: 2

GenotypeDepth
all individuals: 5507
bin: 2.75e1
variant carriers: 9

GenotypeDepth
all individuals: 9241
bin: 3.75e1
variant carriers: 6

GenotypeDepth
all individuals: 8401
bin: 4.25e1
variant carriers: 9

GenotypeDepth
all individuals: 768
bin: 7.25e1
variant carriers: 4

GenotypeQuality
all individuals: 680
bin: 3.25e1
variant carriers: 3

GenotypeQuality
all individuals: 626
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 419
bin: 4.25e1
variant carriers: 6

GenotypeQuality
all individuals: 4094
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2189
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 560
bin: 2.75e1
variant carriers: 9

GenotypeQuality
all individuals: 1418
bin: 7.5e0
variant carriers: 6

GenotypeQuality
all individuals: 848
bin: 2.5e0
variant carriers: 4

GenotypeQuality
all individuals: 641
bin: 3.75e1
variant carriers: 5

GenotypeQuality
all individuals: 2288
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2062
bin: 2.25e1
variant carriers: 10

GenotypeQuality
all individuals: 5848
bin: 6.25e1
variant carriers: 4

GenotypeQuality
all individuals: 940
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4040
bin: 9.25e1
variant carriers: 3

GenotypeQuality
all individuals: 876
bin: 1.25e1
variant carriers: 8

GenotypeQuality
all individuals: 3806
bin: 6.75e1
variant carriers: 4

GenotypeQuality
all individuals: 333
bin: 5.75e1
variant carriers: 5

GenotypeQuality
all individuals: 399
bin: 5.25e1
variant carriers: 4

GenotypeQuality
all individuals: 4003
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 24571
bin: 9.75e1
variant carriers: 20

European (Finnish)
type: Population
allele count: 7
allele frequency: 1.119283658458586e-3
allele num: 6254
num of homozygotes: 0

African
type: Population
allele count: 17
allele frequency: 1.7178658043654e-3
allele num: 9896
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.173708920187793e-4
allele num: 8520
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.826530612244898e-3
allele num: 784
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10544
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.491620111731844e-4
allele num: 11456
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 49
allele frequency: 7.731389441130992e-4
allele num: 63378
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.541e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.235e0

MQRankSum
type: SiteQuality
SIO_000300: 2.51e-1

QD
type: SiteQuality
SIO_000300: 5.600000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.477e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

FS
type: SiteQuality
SIO_000300: 1.604e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.07e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.4e-3

DP
type: SiteQuality
SIO_000300: 2.358663e6

GenotypeDepth
all individuals: 1331
bin: 6.75e1
variant carriers: 2

GenotypeDepth
all individuals: 5480
bin: 2.75e1
variant carriers: 4

GenotypeDepth
all individuals: 783
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 326
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 186
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4219
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2240
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 918
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25921
bin: 9.75e1
variant carriers: 85

GenotypeQuality
all individuals: 578
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3833
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 419
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1316
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1831
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 525
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 809
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4154
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4083
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 423
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5774
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2338
bin: 8.75e1
variant carriers: 1

Latino
type: Population
allele count: 8
allele frequency: 6.960153123368715e-4
allele num: 11494
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10442
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 71
allele frequency: 1.10156080305334e-3
allele num: 64454
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.738994935722633e-5
allele num: 10268
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 5
allele frequency: 7.568876778686043e-4
allele num: 6606
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

MQRankSum
type: SiteQuality
SIO_000300: 1.11e-1

ReadPosRankSum
type: SiteQuality
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DP
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.71e-1

QD
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SIO_000300: 1.318e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.741e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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Latino
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allele frequency: 0.0e0
allele num: 11352
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

African
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allele frequency: 0.0e0
allele num: 8146
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 61340
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.181e1

MQRankSum
type: SiteQuality
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ReadPosRankSum
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ClippingRankSum
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DP
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FS
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.956e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

European (Non-Finnish)
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allele num: 61338
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 8148
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.338099e6

ReadPosRankSum
type: SiteQuality
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MQRankSum
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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FS
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-3

MQ
type: SiteQuality
SIO_000300: 5.939e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 0.0e0
allele num: 8148
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61334
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele num: 8200
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ReadPosRankSum
type: SiteQuality
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MQRankSum
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SIO_000300: -3.55e-1

ClippingRankSum
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MQ
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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SIO_000300: 1.26e0

FS
type: SiteQuality
SIO_000300: 1.254e0

DP
type: SiteQuality
SIO_000300: 7.342074e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8200
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.630310737226516e-5
allele num: 61338
num of homozygotes: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11352
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16008
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.342814e6

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
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BaseQRankSum
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SIO_000300: 1.35e0

FS
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.674e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
allele num: 8200
num of homozygotes: 0

Other
type: Population
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allele num: 842
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Latino
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allele count: 2
allele frequency: 1.761804087385483e-4
allele num: 11352
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61346
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South Asian
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
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QD
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DP
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MQ
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FS
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VQSLOD
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MQRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

Other
type: Population
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African
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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European (Non-Finnish)
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allele num: 61360
num of homozygotes: 0

South Asian
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MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
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FS
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QD
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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DP
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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European (Finnish)
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South Asian
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African
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European (Non-Finnish)
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Latino
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VQSLOD
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MQRankSum
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MQ
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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DP
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FS
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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African
type: Population
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Latino
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South Asian
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European (Finnish)
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European (Non-Finnish)
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allele num: 61390
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QD
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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MQ
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VQSLOD
type: SiteQuality
SIO_000300: -6.125e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 7.354544e6

GenotypeQuality
all individuals: 72
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 242
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4044
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 26
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 16
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 3

GenotypeQuality
all individuals: 23
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 725
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 67
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50604
bin: 9.75e1
variant carriers: 1652

Latino
type: Population
allele count: 386
allele frequency: 3.400281888653982e-2
allele num: 11352
num of homozygotes: 6

Other
type: Population
allele count: 25
allele frequency: 2.969121140142518e-2
allele num: 842
num of homozygotes: 0

African
type: Population
allele count: 213
allele frequency: 2.612214863870493e-2
allele num: 8154
num of homozygotes: 4

South Asian
type: Population
allele count: 34
allele frequency: 2.102659245516388e-3
allele num: 16170
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 9
allele frequency: 1.367365542388332e-3
allele num: 6582
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.219512195121951e-4
allele num: 8200
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1016
allele frequency: 1.654992669815931e-2
allele num: 61390
num of homozygotes: 17

BaseQRankSum
type: SiteQuality
SIO_000300: 3.6e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.36e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.56e0

DP
type: SiteQuality
SIO_000300: 7.488926e6

FS
type: SiteQuality
SIO_000300: 1.097e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.385e0

QD
type: SiteQuality
SIO_000300: 1.204e1

MQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.179999999999999e-1

GenotypeQuality
all individuals: 69
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4159
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50391
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 756
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.62903593653276e-5
allele num: 61386
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16166
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.219512195121951e-4
allele num: 8200
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8154
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.380000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: -1.164e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.896e0

MQRankSum
type: SiteQuality
SIO_000300: 3.37e-1

FS
type: SiteQuality
SIO_000300: 6.121e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.41e0

DP
type: SiteQuality
SIO_000300: 7.336146e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.3e0

MQ
type: SiteQuality
SIO_000300: 5.944e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4150
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50466
bin: 9.75e1
variant carriers: 139

GenotypeQuality
all individuals: 255
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 88
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 753
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8200
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8150
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.761804087385483e-4
allele num: 11352
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.62898286310028e-5
allele num: 61388
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.187648456057007e-3
allele num: 842
num of homozygotes: 0

South Asian
type: Population
allele count: 136
allele frequency: 8.407517309594461e-3
allele num: 16176
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.968e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.38e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.3e-2

QD
type: SiteQuality
SIO_000300: 1.296e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.02e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.0e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.26e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.81e-1

DP
type: SiteQuality
SIO_000300: 7.343333e6

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 540
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4189
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50391
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.25775345321866e-5
allele num: 61392
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8154
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8200
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.809020436927414e-5
allele num: 11352
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16172
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.19e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.11e0

FS
type: SiteQuality
SIO_000300: 2.618e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.91e-1

QD
type: SiteQuality
SIO_000300: 1.069e1

MQ
type: SiteQuality
SIO_000300: 5.962e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 8.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 7.0e-1

DP
type: SiteQuality
SIO_000300: 7.336207e6

GenotypeQuality
all individuals: 552
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 254
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4214
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 87
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50391
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 77
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8200
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8154
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61390
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.809020436927414e-5
allele num: 11352
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16176
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.336374e6

MQ
type: SiteQuality
SIO_000300: 5.97e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -3.596e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.657e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e0

FS
type: SiteQuality
SIO_000300: 8.66e0

MQRankSum
type: SiteQuality
SIO_000300: -2.54e-1

QD
type: SiteQuality
SIO_000300: 1.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.16e0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4218
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50391
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 761
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 82
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.628929793125916e-5
allele num: 61390
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8200
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8154
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16176
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.977e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.9e-2

DP
type: SiteQuality
SIO_000300: 7.336337e6

VQSLOD
type: SiteQuality
SIO_000300: -9.54e-2

FS
type: SiteQuality
SIO_000300: 9.118e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.2e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.57e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.958e0

QD
type: SiteQuality
SIO_000300: 1.226e1

GenotypeQuality
all individuals: 562
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 50391
bin: 9.75e1
variant carriers: 15

GenotypeQuality
all individuals: 4223
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 82
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 760
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16176
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.62887672660933e-5
allele num: 61392
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8200
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8154
num of homozygotes: 0

Latino
type: Population
allele count: 14
allele frequency: 1.233262861169838e-3
allele num: 11352
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.8e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.99e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.66e-1

QD
type: SiteQuality
SIO_000300: 1.419e1

MQ
type: SiteQuality
SIO_000300: 6.082e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

DP
type: SiteQuality
SIO_000300: 7.337639e6

VQSLOD
type: SiteQuality
SIO_000300: 3.6e0

GenotypeQuality
all individuals: 18
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50388
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 563
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 82
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4226
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8200
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16178
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8154
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.812125484666901e-5
allele num: 11348
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.257859586251833e-5
allele num: 61390
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.33e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

DP
type: SiteQuality
SIO_000300: 7.3371e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.41e-1

QD
type: SiteQuality
SIO_000300: 1.064e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.69e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.4e-2

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61390
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16180
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8154
num of homozygotes: 0

Latino
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allele count: 3
allele frequency: 2.642706131078224e-4
allele num: 11352
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8200
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.64e-1

DP
type: SiteQuality
SIO_000300: 7.336109e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

MQ
type: SiteQuality
SIO_000300: 5.996e1

VQSLOD
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QD
type: SiteQuality
SIO_000300: 1.24e1

ClippingRankSum
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SIO_000300: -3.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e-1

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 8154
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.629195177582274e-5
allele num: 61380
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11352
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
SIO_000300: -7.84e-1

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 7.335527e6

FS
type: SiteQuality
SIO_000300: 5.5e-1

VQSLOD
type: SiteQuality
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BaseQRankSum
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MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -1.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

ReadPosRankSum
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SIO_000300: 7.85e-1

GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11352
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

European (Non-Finnish)
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allele count: 14
allele frequency: 2.280947570790837e-4
allele num: 61378
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8200
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16158
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8154
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.34e0

FS
type: SiteQuality
SIO_000300: 2.898e0

BaseQRankSum
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SIO_000300: -2.471e0

MQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.97e1

QD
type: SiteQuality
SIO_000300: 1.261e1

InbreedingCoeff
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SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 7.335575e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.86e-1

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

African
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allele count: 2
allele frequency: 2.452783909737552e-4
allele num: 8154
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11352
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.199628022318661e-5
allele num: 16130
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8200
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61364
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.99e1

DP
type: SiteQuality
SIO_000300: 7.330434e6

FS
type: SiteQuality
SIO_000300: 7.05e-1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.45e1

BaseQRankSum
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SIO_000300: 6.47e0

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 3
allele frequency: 1.864743908503232e-4
allele num: 16088
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8154
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8200
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61346
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11352
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
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DP
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MQ
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.326e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 11352
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8202
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 6.25e-5
allele num: 16000
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61326
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
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FS
type: SiteQuality
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MQRankSum
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InbreedingCoeff
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MQ
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
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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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bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16002
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61322
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8154
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8200
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European (Finnish)
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allele count: 1
allele frequency: 1.519295047098146e-4
allele num: 6582
num of homozygotes: 0

Other
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allele count: 0
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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ReadPosRankSum
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QD
type: SiteQuality
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ClippingRankSum
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BaseQRankSum
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
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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bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

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

African
type: Population
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num of homozygotes: 0

Other
type: Population
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Latino
type: Population
allele count: 1
allele frequency: 8.809020436927414e-5
allele num: 11352
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8202
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61320
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
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ReadPosRankSum
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ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
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DP
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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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 7.25e1
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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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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15962
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61314
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8154
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8202
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.809020436927414e-5
allele num: 11352
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 6.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.419e0

DP
type: SiteQuality
SIO_000300: 7.317162e6

MQ
type: SiteQuality
SIO_000300: 5.884e1

MQRankSum
type: SiteQuality
SIO_000300: 7.9e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.88e-1

QD
type: SiteQuality
SIO_000300: 1.811e1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10326
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506795648374167e-5
allele num: 66366
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 3.52e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.47e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

FS
type: SiteQuality
SIO_000300: 2.613e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.01e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.565e0

DP
type: SiteQuality
SIO_000300: 1.676716e6

QD
type: SiteQuality
SIO_000300: 1.142e1

GenotypeQuality
all individuals: 114
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8742
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10330
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.653513326410523e-5
allele num: 11556
num of homozygotes: 0

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

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

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

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

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

FS
type: SiteQuality
SIO_000300: 2.281e0

VQSLOD
type: SiteQuality
SIO_000300: 6.929999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.285e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.39e-1

QD
type: SiteQuality
SIO_000300: 1.174e1

MQRankSum
type: SiteQuality
SIO_000300: -5.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.35e-1

DP
type: SiteQuality
SIO_000300: 1.677167e6

GenotypeQuality
all individuals: 1142
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8732
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 399
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variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 9.25e1
variant carriers: 1

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

Other
type: Population
allele count: 1
allele frequency: 1.106194690265487e-3
allele num: 904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.20536386921802e-4
allele num: 66370
num of homozygotes: 0

African
type: Population
allele count: 98
allele frequency: 9.486931268151016e-3
allele num: 10330
num of homozygotes: 0

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

Latino
type: Population
allele count: 10
allele frequency: 8.653513326410523e-4
allele num: 11556
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 4.59e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.4e-1

FS
type: SiteQuality
SIO_000300: 6.08e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.9e-3

DP
type: SiteQuality
SIO_000300: 1.678315e6

MQRankSum
type: SiteQuality
SIO_000300: 2.78e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.892e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.78e-1

QD
type: SiteQuality
SIO_000300: 1.209e1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.01050666827227e-5
allele num: 66434
num of homozygotes: 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: 8592
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.11e0

VQSLOD
type: SiteQuality
SIO_000300: 8.400000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e0

QD
type: SiteQuality
SIO_000300: 1.106e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.419999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.675747e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -9.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 6.22e-1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1442
bin: 9.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505253334136135e-5
allele num: 66434
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.667440061871617e-5
allele num: 10344
num of homozygotes: 0

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.18e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.89e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.0e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.93e0

FS
type: SiteQuality
SIO_000300: 2.157e0

QD
type: SiteQuality
SIO_000300: 1.171e1

MQ
type: SiteQuality
SIO_000300: 5.963e1

DP
type: SiteQuality
SIO_000300: 1.675883e6

GenotypeQuality
all individuals: 1438
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 391
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variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 3.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66480
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.656237929702588e-5
allele num: 10356
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.35e-1

QD
type: SiteQuality
SIO_000300: 1.262e1

MQ
type: SiteQuality
SIO_000300: 5.945e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 4.37e-1

DP
type: SiteQuality
SIO_000300: 1.67736e6

VQSLOD
type: SiteQuality
SIO_000300: -2.04e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.474e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.61e-1

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 2.25e1
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GenotypeQuality
all individuals: 25
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 392
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variant carriers: 0

GenotypeQuality
all individuals: 2433
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66480
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
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QD
type: SiteQuality
SIO_000300: 1.285e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.79e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.959e1