7-72951689-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72951689
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72951689
    reference: chr 7
allele count: 1
allele frequency: 8.293524416135881e-6
allele num: 120576
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*282C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.560C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.548C>T
  hgvsp: ENSP00000223368.2:p.Pro183Leu
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.456C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.257C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*577C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*184C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*292C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.799C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.377C>T
  hgvsp: ENSP00000393230.1:p.Pro126Leu
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.401C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.667C>T
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7690
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21874
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15749
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3649
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2036
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6546
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro183Leu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ

7-72951700-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72951700
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72951700
    reference: chr 7
allele count: 2
allele frequency: 1.6604400166044e-5
allele num: 120450
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*173C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.445C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*271C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*566C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.537C>T
  hgvsp: ENST00000223368.2:c.537C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.366C>T
  hgvsp: ENST00000411832.1:c.366C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*281C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.788C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.549C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.246C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.656C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.390C>T
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7618
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21828
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3645
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2036
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15722
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6534
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp179Asp
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff

7-72951704-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72951704
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72951704
    reference: chr 7
allele count: 2
allele frequency: 1.661626399920242e-5
allele num: 120364
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.545A>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.533A>T
  hgvsp: ENSP00000223368.2:p.Glu178Val
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*169A>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.784A>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.652A>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.441A>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*267A>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*277A>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.362A>T
  hgvsp: ENSP00000393230.1:p.Glu121Val
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*562A>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.242A>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.386A>T
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7535
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21799
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6534
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3643
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu178Val
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

7-72951706-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72951706
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72951706
    reference: chr 7
allele count: 1
allele frequency: 8.310203267571925e-6
allele num: 120334
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*167G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.384G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*275G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*265G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.531G>C
  hgvsp: ENSP00000223368.2:p.Glu177Asp
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.360G>C
  hgvsp: ENSP00000393230.1:p.Glu120Asp
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.240G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.782G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.650G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.439G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.543G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*560G>C
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2036
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21802
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6536
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7499
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15702
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3642
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Glu177Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

7-72951716-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72951716
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72951716
    reference: chr 7
allele count: 1
allele frequency: 8.329723786359244e-6
allele num: 120052
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.429T>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.640T>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.521T>C
  hgvsp: ENSP00000223368.2:p.Val174Ala
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*255T>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*265T>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.374T>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*550T>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.533T>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.772T>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.350T>C
  hgvsp: ENSP00000393230.1:p.Val117Ala
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.230T>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*157T>C
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15652
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3637
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6522
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21667
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val174Ala
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

7-72951717-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72951717
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72951717
    reference: chr 7
allele count: 1
allele frequency: 8.330417687142833e-6
allele num: 120042
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*254G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.229G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.373G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.349G>A
  hgvsp: ENSP00000393230.1:p.Val117Ile
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.520G>A
  hgvsp: ENSP00000223368.2:p.Val174Ile
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.532G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*264G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*156G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.771G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.639G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*549G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.428G>A
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7208
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6525
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21660
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3640
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val174Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP

7-72951718-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72951718
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72951718
    reference: chr 7
allele count: 2
allele frequency: 1.666361167119361e-5
allele num: 120022
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.770C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*263C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.519C>T
  hgvsp: ENST00000223368.2:c.519C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.638C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*253C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*155C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.228C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*548C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.348C>T
  hgvsp: ENST00000411832.1:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.372C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.427C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.531C>T
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3635
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15642
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21632
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7187
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.519C>T
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum

7-72951718-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72951718
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72951718
    reference: chr 7
allele count: 14
allele frequency: 1.166452816983553e-4
allele num: 120022
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.638C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*263C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*155C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*253C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*548C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.228C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.372C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.427C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.770C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.531C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.348C>A
  hgvsp: ENST00000411832.1:c.348C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.519C>A
  hgvsp: ENST00000223368.2:c.519C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3635
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21632
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7187
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 15642
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.519C>A
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

7-72951725-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72951725
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72951725
    reference: chr 7
allele count: 1
allele frequency: 8.353939717970996e-6
allele num: 119704
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-5C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.517-5C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.346-5C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.529-5C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.425-5C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.636-5C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.370-5C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*251-5C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*153-5C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*546-5C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.768-5C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*261-5C>T
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6790
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15542
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21276
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.517-5C>T
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

7-72951732-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72951732
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72951732
    reference: chr 7
allele count: 2
allele frequency: 1.672856234735187e-5
allele num: 119556
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-12G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*261-12G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.370-12G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.529-12G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.636-12G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.768-12G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*251-12G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*546-12G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.346-12G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*153-12G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.517-12G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.425-12G>C
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6672
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21118
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15433
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3623
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/7-72951735-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72951735
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72951735
    reference: chr 7
allele count: 2
allele frequency: 1.674817444898506e-5
allele num: 119416
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.529-15T>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-15T>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.370-15T>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.636-15T>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.346-15T>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.425-15T>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*153-15T>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*546-15T>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*251-15T>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.517-15T>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*261-15T>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.768-15T>G
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6490
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6461
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15326
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2025
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20869
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3612
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP

7-72951737-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72951737
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72951737
    reference: chr 7
allele count: 1
allele frequency: 8.389120987902887e-6
allele num: 119202
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.529-17G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-17G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*546-17G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.517-17G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*261-17G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.370-17G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.346-17G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.768-17G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*251-17G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.636-17G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*153-17G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.425-17G>A
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6424
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3605
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15135
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6127
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP

7-72951741-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72951741
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72951741
    reference: chr 7
allele count: 1
allele frequency: 8.40039649871474e-6
allele num: 119042
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.529-21C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.517-21C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.346-21C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.425-21C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*153-21C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.768-21C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.370-21C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*546-21C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*261-21C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.636-21C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*251-21C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-21C>A
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3203
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20076
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5896
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14832
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6333
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2016
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

7-72951744-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72951744
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72951744
    reference: chr 7
allele count: 1
allele frequency: 8.407317729351627e-6
allele num: 118944
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.346-24A>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.425-24A>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*153-24A>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.636-24A>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-24A>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*261-24A>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*251-24A>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*546-24A>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.370-24A>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.529-24A>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.768-24A>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.517-24A>T
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14586
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3575
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19727
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5804
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3577
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6279
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2012
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ

7-72951753-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72951753
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72951753
    reference: chr 7
allele count: 1
allele frequency: 8.443236123541432e-6
allele num: 118438
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*261-33G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*153-33G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.768-33G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.346-33G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*546-33G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*251-33G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.636-33G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.529-33G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.425-33G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.517-33G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.370-33G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-33G>A
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5127
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3511
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12967
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5163
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5204
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17228
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5946
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS

http://identifiers.org/exac.variant/7-72951755-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72951755
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72951755
    reference: chr 7
allele count: 1
allele frequency: 8.459091831900928e-6
allele num: 118216
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*251-35G>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*546-35G>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.529-35G>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.768-35G>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.346-35G>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.517-35G>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.425-35G>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*153-35G>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-35G>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*261-35G>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.636-35G>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.370-35G>T
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6530
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3494
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5795
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5280
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5397
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16396
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

7-72951759-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72951759
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72951759
    reference: chr 7
allele count: 1
allele frequency: 8.475869200386499e-6
allele num: 117982
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*261-39A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.425-39A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.636-39A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*251-39A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.768-39A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-39A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.370-39A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.346-39A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.529-39A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*153-39A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*546-39A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.517-39A>G
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7790
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11591
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5312
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15538
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5565
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5715
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3474
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

7-72951764-ACCAGAACCTTC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72951764
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72951753
    reference: chr 7
allele count: 4
allele frequency: 3.404371212637026e-5
allele num: 117496
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 13205
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3444
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5261
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1969
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9051
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10180
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5548
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2054
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: ACCAGAACCTTC
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

7-72951766-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72951766
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72951766
    reference: chr 7
allele count: 1
allele frequency: 8.541314337450248e-6
allele num: 117078
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-46G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.517-46G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.529-46G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.768-46G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*251-46G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.346-46G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.636-46G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*261-46G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.425-46G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*546-46G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.370-46G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*153-46G>C
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9360
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5456
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5211
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9019
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11983
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10201
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3437
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

7-72951772-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72951772
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72951772
    reference: chr 7
allele count: 2
allele frequency: 1.72084459052503e-5
allele num: 116222
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.517-52G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.346-52G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.636-52G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-52G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*251-52G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.529-52G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.768-52G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*153-52G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*261-52G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.370-52G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.425-52G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*546-52G>C
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11344
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8494
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8938
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5226
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11774
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/7-72952215-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72952215
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72952215
    reference: chr 7
allele count: 1
allele frequency: 8.972150445018663e-6
allele num: 111456
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*250+49G>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*260+49G>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.345+49G>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.369+49G>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*152+49G>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.424+49G>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.767+49G>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*545+49G>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.528+49G>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-495G>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.635+49G>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.516+49G>T
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3205
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7451
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8044
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5128
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9914
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10676
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2591
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3670
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ

7-72952217-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72952217
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72952217
    reference: chr 7
allele count: 1
allele frequency: 8.957202486519411e-6
allele num: 111642
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.424+47A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.369+47A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.767+47A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*250+47A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.635+47A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-497A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.345+47A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.528+47A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*545+47A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.516+47A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*152+47A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*260+47A>G
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10757
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7459
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5147
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2565
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10068
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3492
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2736
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8751
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3204
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/7-72952223-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72952223
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72952222
    reference: chr 7
allele count: 1
allele frequency: 8.972311446874944e-6
allele num: 111454
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*152+40delT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.767+40delT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*545+40delT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.424+40delT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-504delT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*250+40delT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.369+40delT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*260+40delT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.345+40delT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.516+40delT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.635+40delT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.528+40delT
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9844
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7622
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11131
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3521
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10755
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5259
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: CA
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/7-72952227-AAAAC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72952227
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72952223
    reference: chr 7
allele count: 1
allele frequency: 8.883834973881526e-6
allele num: 112564
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.424+33_424+36delGTTT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.345+33_345+36delGTTT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.767+33_767+36delGTTT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*260+33_*260+36delGTTT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*250+33_*250+36delGTTT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.516+33_516+36delGTTT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.369+33_369+36delGTTT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*545+33_*545+36delGTTT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.635+33_635+36delGTTT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*152+33_*152+36delGTTT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-511_226-508delGTTT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.528+33_528+36delGTTT
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 3570
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1726
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11389
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10517
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10849
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7690
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5214
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: AAAAC
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/7-72952231-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72952231
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72952232
    reference: chr 7
allele count: 1
allele frequency: 8.871697510601678e-6
allele num: 112718
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.345+32dupT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*152+32dupT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.424+32dupT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*250+32dupT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.369+32dupT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*260+32dupT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.767+32dupT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*545+32dupT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-512dupT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.635+32dupT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.516+32dupT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.528+32dupT
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11483
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3549
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10906
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7703
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5228
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1933
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/7-72952232-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72952232
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72952232
    reference: chr 7
allele count: 1
allele frequency: 8.851437473445687e-6
allele num: 112976
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.528+32T>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-512T>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*545+32T>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.345+32T>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.635+32T>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*250+32T>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*152+32T>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.767+32T>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.424+32T>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.369+32T>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*260+32T>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.516+32T>G
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10964
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7705
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3562
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10907
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3255
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11498
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5219
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/7-72952248-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72952248
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72952249
    reference: chr 7
allele count: 3
allele frequency: 2.617709678545251e-5
allele num: 114604
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*260+15dupT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.516+15dupT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*250+15dupT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-529dupT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.767+15dupT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*152+15dupT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.528+15dupT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.369+15dupT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.424+15dupT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.635+15dupT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.345+15dupT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*545+15dupT
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11682
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3082
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12065
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5220
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10958
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
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: C
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/7-72952248-CAA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72952248
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72952246
    reference: chr 7
allele count: 9
allele frequency: 7.853129035635754e-5
allele num: 114604
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-530_226-529delTT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*152+14_*152+15delTT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*260+14_*260+15delTT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.635+14_635+15delTT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.528+14_528+15delTT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.345+14_345+15delTT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.767+14_767+15delTT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.424+14_424+15delTT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*545+14_*545+15delTT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.516+14_516+15delTT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*250+14_*250+15delTT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.369+14_369+15delTT
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5220
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12065
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3082
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10958
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11682
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7706
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: CAA
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP

7-72952250-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72952250
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72952250
    reference: chr 7
allele count: 1
allele frequency: 8.694291328313829e-6
allele num: 115018
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*250+14T>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*152+14T>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-530T>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*545+14T>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.516+14T>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.635+14T>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.767+14T>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.345+14T>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.369+14T>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*260+14T>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.424+14T>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.528+14T>C
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2943
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10963
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11700
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12326
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5220
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7709
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

7-72952252-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72952252
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72952252
    reference: chr 7
allele count: 1
allele frequency: 8.674832575731289e-6
allele num: 115276
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.767+12C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*152+12C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-532C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.345+12C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.516+12C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*250+12C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.424+12C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.528+12C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.369+12C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.635+12C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*260+12C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*545+12C>T
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5221
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7710
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3259
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12488
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11718
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2838
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

7-72952257-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72952257
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72952257
    reference: chr 7
allele count: 1
allele frequency: 8.620541025154739e-6
allele num: 116002
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.767+7A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.635+7A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.516+7A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.424+7A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*250+7A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*260+7A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.369+7A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*545+7A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.345+7A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.528+7A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*152+7A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-537A>G
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2529
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5220
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7711
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12928
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3259
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.516+7A>G
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

7-72952258-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72952258
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72952258
    reference: chr 7
allele count: 3
allele frequency: 2.582955934771753e-5
allele num: 116146
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*152+6C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.528+6C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.345+6C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.767+6C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.516+6C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.635+6C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*250+6C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.424+6C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*545+6C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-538C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*260+6C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.369+6C>A
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3259
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11793
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10968
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13013
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7713
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.516+6C>A
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

7-72952268-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72952268
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72952268
    reference: chr 7
allele count: 8
allele frequency: 6.789327177676693e-5
allele num: 117832
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*541C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*256C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-548C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*246C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.524C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.512C>T
  hgvsp: ENSP00000223368.2:p.Thr171Ile
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.763C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*148C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.365C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.631C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.420C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.341C>T
  hgvsp: ENSP00000393230.1:p.Thr114Ile
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10993
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5221
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11967
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13894
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7710
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3259
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr171Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD

7-72952269-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72952269
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72952269
    reference: chr 7
allele count: 1
allele frequency: 8.480037990570198e-6
allele num: 117924
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.511A>G
  hgvsp: ENSP00000223368.2:p.Thr171Ala
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*540A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.630A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*245A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*147A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.762A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.364A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*255A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-549A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.419A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.340A>G
  hgvsp: ENSP00000393230.1:p.Thr114Ala
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.523A>G
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3259
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10996
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11976
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13964
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr171Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
reference allele: T
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD

7-72952273-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72952273
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72952273
    reference: chr 7
allele count: 1
allele frequency: 8.44409166905916e-6
allele num: 118426
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*241A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.519A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-553A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.758A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.360A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.415A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*251A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*143A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*536A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.336A>G
  hgvsp: ENST00000411832.1:c.336A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.507A>G
  hgvsp: ENST00000223368.2:c.507A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.626A>G
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10999
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14204
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3259
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12027
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7715
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu169Leu
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

7-72952276-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72952276
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72952276
    reference: chr 7
allele count: 10
allele frequency: 8.425309630128907e-5
allele num: 118690
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*248A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.504A>G
  hgvsp: ENST00000223368.2:c.504A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*140A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-556A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.516A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.357A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.623A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*533A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.755A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.333A>G
  hgvsp: ENST00000411832.1:c.333A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*238A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.412A>G
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12063
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14316
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7709
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11007
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Pro168Pro
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: ClippingRankSum

7-72952291-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72952291
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72952291
    reference: chr 7
allele count: 1
allele frequency: 8.372965369415233e-6
allele num: 119432
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*233G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.318G>A
  hgvsp: ENST00000411832.1:c.318G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.489G>A
  hgvsp: ENST00000223368.2:c.489G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*125G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.608G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.342G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*223G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*518G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.740G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-571G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.397G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.501G>A
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11025
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14661
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12192
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7714
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys163Lys
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

7-72952306-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72952306
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72952306
    reference: chr 7
allele count: 2
allele frequency: 1.673640167364017e-5
allele num: 119500
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.593T>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*503T>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.486T>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*218T>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*208T>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.725T>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.382T>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.474T>A
  hgvsp: ENST00000223368.2:c.474T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*110T>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.327T>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-586T>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.303T>A
  hgvsp: ENST00000411832.1:c.303T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14521
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7716
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12289
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro158Pro
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

7-72952323-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72952323
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72952323
    reference: chr 7
allele count: 1
allele frequency: 8.397997917296517e-6
allele num: 119076
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.469G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.365G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*93G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.708G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*486G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.286G>C
  hgvsp: ENSP00000393230.1:p.Glu96Gln
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*201G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*191G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.310G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.457G>C
  hgvsp: ENSP00000223368.2:p.Glu153Gln
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-603G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.576G>C
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7716
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12306
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13699
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11012
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu153Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum

7-72952324-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72952324
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72952324
    reference: chr 7
allele count: 1
allele frequency: 8.399973120086016e-6
allele num: 119048
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.285G>A
  hgvsp: ENST00000411832.1:c.285G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.707G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-604G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*190G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*485G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.456G>A
  hgvsp: ENST00000223368.2:c.456G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*92G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*200G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.468G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.309G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.364G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.575G>A
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11016
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7719
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12297
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13699
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser152Ser
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

7-72952327-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72952327
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72952327
    reference: chr 7
allele count: 3
allele frequency: 2.52989492503078e-5
allele num: 118582
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.572C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-607C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.282C>T
  hgvsp: ENST00000411832.1:c.282C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.465C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*482C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*197C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*187C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.453C>T
  hgvsp: ENST00000223368.2:c.453C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.361C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*89C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.306C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.704C>T
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7716
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12252
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3257
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12917
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser151Ser
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

7-72952328-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72952328
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72952328
    reference: chr 7
allele count: 1
allele frequency: 8.43340979624882e-6
allele num: 118576
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.305C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*196C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*88C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.452C>T
  hgvsp: ENSP00000223368.2:p.Ser151Phe
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.360C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*481C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-608C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*186C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.571C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.281C>T
  hgvsp: ENSP00000393230.1:p.Ser94Phe
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.464C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.703C>T
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7716
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11004
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12928
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12256
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser151Phe
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

7-72952337-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72952337
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72952337
    reference: chr 7
allele count: 3
allele frequency: 2.535496957403651e-5
allele num: 118320
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*187C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-617C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.272C>T
  hgvsp: ENSP00000393230.1:p.Ser91Phe
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*177C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.351C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*79C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.562C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.443C>T
  hgvsp: ENSP00000223368.2:p.Ser148Phe
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.694C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.296C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*472C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.455C>T
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7715
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12596
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10998
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1408
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12119
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser148Phe
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum

7-72952351-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72952351
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72952351
    reference: chr 7
allele count: 3
allele frequency: 2.552018646749579e-5
allele num: 117554
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.449-8C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.556-8C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.345-8C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*466-8C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.688-8C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*171-8C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-631C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.266-8C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.437-8C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*181-8C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.282C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*73-8C>T
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11529
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10980
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11899
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7715
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5224
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.437-8C>T
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum

7-72952359-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72952359
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72952359
    reference: chr 7
allele count: 1
allele frequency: 8.558566268978621e-6
allele num: 116842
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.449-16C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.266-16C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.274C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*171-16C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.688-16C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.345-16C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.437-16C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*73-16C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*466-16C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-639C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.556-16C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*181-16C>T
  variant of: http://identifiers.org/hgnc/1005
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7721
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1835
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10961
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2536
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10999
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11768
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
reference allele: G
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff

7-72952359-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72952359
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72952359
    reference: chr 7
allele count: 1
allele frequency: 8.558566268978621e-6
allele num: 116842
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.556-16C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.688-16C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.266-16C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.437-16C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*73-16C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*466-16C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.274C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.345-16C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-639C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.449-16C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*171-16C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*181-16C>A
  variant of: http://identifiers.org/hgnc/1005
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7721
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2536
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10999
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10961
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1835
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11768
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD

7-72952362-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72952362
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72952362
    reference: chr 7
allele count: 4
allele frequency: 3.436957605127941e-5
allele num: 116382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.271G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.449-19G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-642G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*73-19G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.266-19G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*181-19G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.688-19G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*466-19G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*171-19G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.556-19G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.437-19G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.345-19G>A
  variant of: http://identifiers.org/hgnc/1005
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10866
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1906
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5229
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11711
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2567
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7722
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1933
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD

7-72952363-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72952363
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72952363
    reference: chr 7
allele count: 1
allele frequency: 8.598156555234557e-6
allele num: 116304
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*466-20C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*73-20C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*181-20C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.437-20C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*171-20C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.345-20C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.556-20C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.270C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-643C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.266-20C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.688-20C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.449-20C>T
  variant of: http://identifiers.org/hgnc/1005
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2562
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1974
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7722
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10786
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10953
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5231
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11696
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

7-72952365-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72952365
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72952365
    reference: chr 7
allele count: 1
allele frequency: 8.609111884018045e-6
allele num: 116156
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*466-22G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*181-22G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.266-22G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*171-22G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-645G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.345-22G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*73-22G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.449-22G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.268G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.688-22G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.556-22G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.437-22G>A
  variant of: http://identifiers.org/hgnc/1005
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3259
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5231
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11704
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10702
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7723
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2590
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10962
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP

7-72952371-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72952371
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72952371
    reference: chr 7
allele count: 1
allele frequency: 8.642444774777888e-6
allele num: 115708
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.437-28C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.262C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*171-28C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.556-28C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*466-28C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.449-28C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*73-28C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.688-28C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.345-28C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*181-28C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-651C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.266-28C>T
  variant of: http://identifiers.org/hgnc/1005
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5231
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2195
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7722
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10968
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11652
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10296
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ

7-72952373-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72952373
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72952373
    reference: chr 7
allele count: 1
allele frequency: 8.672274737663689e-6
allele num: 115310
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.260G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*181-30G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.556-30G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.688-30G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-653G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*171-30G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.345-30G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*73-30G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.437-30G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*466-30G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.266-30G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.449-30G>A
  variant of: http://identifiers.org/hgnc/1005
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10105
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7724
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2253
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11622
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5238
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3265
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10964
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

7-72952378-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72952378
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72952378
    reference: chr 7
allele count: 2
allele frequency: 1.740038280842178e-5
allele num: 114940
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.266-35G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.255G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*466-35G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.556-35G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.437-35G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.449-35G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*171-35G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-658G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.688-35G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*181-35G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*73-35G>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.345-35G>C
  variant of: http://identifiers.org/hgnc/1005
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2552
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7726
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11538
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5243
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9681
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10923
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff

7-72952382-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72952382
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72952382
    reference: chr 7
allele count: 1
allele frequency: 8.719612151651495e-6
allele num: 114684
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.449-39G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.688-39G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*171-39G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.251G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.556-39G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-662G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*73-39G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.437-39G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*466-39G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.266-39G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*181-39G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.345-39G>A
  variant of: http://identifiers.org/hgnc/1005
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10880
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1983
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2516
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3273
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2480
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7721
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9249
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD

7-72952383-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72952383
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72952383
    reference: chr 7
allele count: 1
allele frequency: 8.717787774174425e-6
allele num: 114708
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.449-40G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*466-40G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.437-40G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.266-40G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.250G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*171-40G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-663G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.556-40G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.688-40G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*73-40G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*181-40G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.345-40G>A
  variant of: http://identifiers.org/hgnc/1005
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11402
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2476
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9237
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1934
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10884
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1978
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5249
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7724
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3275
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2525
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

7-72952391-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72952391
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72952391
    reference: chr 7
allele count: 1
allele frequency: 8.755034144633164e-6
allele num: 114220
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.266-48A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.345-48A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*73-48A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.556-48A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*181-48A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.437-48A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*171-48A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.688-48A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.242A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.449-48A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*466-48A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.226-671A>G
  variant of: http://identifiers.org/hgnc/1005
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7716
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9464
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2325
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2738
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10702
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

7-72954173-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72954173
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72954173
    reference: chr 7
allele count: 1
allele frequency: 8.515131388477325e-6
allele num: 117438
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*170+39G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*465+39G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.436+39G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.687+39G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.266-1830G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493592
  gene symbol: BCL7B
  hgvsc: ENST00000493592.1:n.455G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*180+39G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.345-1830G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.448+39G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.555+39G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.64+39G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*72+39G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.225+39G>A
  variant of: http://identifiers.org/hgnc/1005
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1592
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2686
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22486
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3714
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21726
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4916
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

7-72954176-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72954176
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72954176
    reference: chr 7
allele count: 1
allele frequency: 8.492713252029759e-6
allele num: 117748
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*465+36A>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*72+36A>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.687+36A>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493592
  gene symbol: BCL7B
  hgvsc: ENST00000493592.1:n.452A>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.448+36A>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*180+36A>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*170+36A>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.225+36A>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.64+36A>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.266-1833A>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.436+36A>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.555+36A>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.345-1833A>C
  variant of: http://identifiers.org/hgnc/1005
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3194
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22827
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22831
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD

7-72954182-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72954182
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72954181
    reference: chr 7
allele count: 1
allele frequency: 8.463960456376747e-6
allele num: 118148
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493592
  gene symbol: BCL7B
  hgvsc: ENST00000493592.1:n.445delT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*72+29delT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.345-1840delT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*170+29delT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.64+29delT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.448+29delT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*465+29delT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.687+29delT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*180+29delT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.555+29delT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.225+29delT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.266-1840delT
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.436+29delT
  variant of: http://identifiers.org/hgnc/1005
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2245
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5020
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: GA
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD

7-72954187-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72954187
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72954187
    reference: chr 7
allele count: 28
allele frequency: 2.3639863564216e-4
allele num: 118444
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.345-1844A>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*180+25A>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.555+25A>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.64+25A>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*170+25A>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.225+25A>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.448+25A>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.266-1844A>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.436+25A>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493592
  gene symbol: BCL7B
  hgvsc: ENST00000493592.1:n.441A>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*465+25A>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*72+25A>C
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.687+25A>C
  variant of: http://identifiers.org/hgnc/1005
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24878
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 23656
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 3.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

7-72954194-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72954194
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72954194
    reference: chr 7
allele count: 1
allele frequency: 8.409580193756727e-6
allele num: 118912
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.345-1851G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*180+18G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*170+18G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493592
  gene symbol: BCL7B
  hgvsc: ENST00000493592.1:n.434G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.436+18G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.555+18G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.448+18G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*465+18G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.64+18G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*72+18G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.266-1851G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.687+18G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.225+18G>A
  variant of: http://identifiers.org/hgnc/1005
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25104
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5193
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24240
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ

7-72954195-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72954195
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72954195
    reference: chr 7
allele count: 4
allele frequency: 3.358127508101483e-5
allele num: 119114
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.64+17C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*72+17C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493592
  gene symbol: BCL7B
  hgvsc: ENST00000493592.1:n.433C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*170+17C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.225+17C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*180+17C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.555+17C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.345-1852C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.436+17C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.266-1852C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.687+17C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*465+17C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.448+17C>T
  variant of: http://identifiers.org/hgnc/1005
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25205
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24359
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5208
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

7-72954195-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72954195
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72954195
    reference: chr 7
allele count: 1
allele frequency: 8.395318770253707e-6
allele num: 119114
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.345-1852C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*170+17C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*180+17C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.225+17C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493592
  gene symbol: BCL7B
  hgvsc: ENST00000493592.1:n.433C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*72+17C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.64+17C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.687+17C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.555+17C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*465+17C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.266-1852C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.436+17C>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.448+17C>A
  variant of: http://identifiers.org/hgnc/1005
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5208
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24359
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff

7-72954197-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72954197
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72954197
    reference: chr 7
allele count: 1
allele frequency: 8.386869517084054e-6
allele num: 119234
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.266-1854G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.225+15G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.345-1854G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*465+15G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*180+15G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.687+15G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.436+15G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493592
  gene symbol: BCL7B
  hgvsc: ENST00000493592.1:n.431G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.64+15G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.448+15G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.555+15G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*170+15G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*72+15G>A
  variant of: http://identifiers.org/hgnc/1005
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5250
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24558
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

7-72954205-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72954205
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72954205
    reference: chr 7
allele count: 2
allele frequency: 1.669588446447951e-5
allele num: 119790
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.266-1862C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.225+7C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.64+7C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*170+7C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493592
  gene symbol: BCL7B
  hgvsc: ENST00000493592.1:n.423C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.436+7C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*72+7C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*180+7C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*465+7C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.555+7C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.687+7C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.345-1862C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.448+7C>T
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24948
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5341
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.436+7C>T
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

7-72954234-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72954234
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72954234
    reference: chr 7
allele count: 2
allele frequency: 1.660826094899603e-5
allele num: 120422
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.266-1891G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.426G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*158G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.414G>A
  hgvsp: ENST00000223368.2:c.414G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.203G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.345-1891G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.533G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*443G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493592
  gene symbol: BCL7B
  hgvsc: ENST00000493592.1:n.394G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*50G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.42G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000481667
  gene symbol: BCL7B
  hgvsc: ENST00000481667.1:n.495G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.665G>A
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*148G>A
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25056
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5442
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25645
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr138Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

7-72954235-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72954235
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72954235
    reference: chr 7
allele count: 1
allele frequency: 8.302889405513118e-6
allele num: 120440
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*147C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.413C>T
  hgvsp: ENSP00000223368.2:p.Thr138Met
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.41C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000481667
  gene symbol: BCL7B
  hgvsc: ENST00000481667.1:n.494C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.425C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*157C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.266-1892C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*442C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*49C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.532C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.345-1892C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.664C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.202C>T
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493592
  gene symbol: BCL7B
  hgvsc: ENST00000493592.1:n.393C>T
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25044
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5436
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25682
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr138Met
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: QD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

7-72954236-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72954236
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 72954236
    reference: chr 7
allele count: 5
allele frequency: 4.151168969181722e-5
allele num: 120448
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000486818
  gene symbol: BCL7B
  hgvsc: ENST00000486818.1:n.40A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493592
  gene symbol: BCL7B
  hgvsc: ENST00000493592.1:n.392A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000464288
  gene symbol: BCL7B
  hgvsc: ENST00000464288.1:n.424A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000411073
  ensembl transcript: ENST00000455335
  gene symbol: BCL7B
  hgvsc: ENST00000455335.1:c.*441A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414231
  ensembl transcript: ENST00000448175
  gene symbol: BCL7B
  hgvsc: ENST00000448175.1:c.*156A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000223368
  ensembl transcript: ENST00000223368
  gene symbol: BCL7B
  hgvsc: ENST00000223368.2:c.412A>G
  hgvsp: ENSP00000223368.2:p.Thr138Ala
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000406069
  ensembl transcript: ENST00000416906
  gene symbol: BCL7B
  hgvsc: ENST00000416906.1:c.*146A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493671
  gene symbol: BCL7B
  hgvsc: ENST00000493671.1:n.663A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000414473
  ensembl transcript: ENST00000454871
  gene symbol: BCL7B
  hgvsc: ENST00000454871.1:c.*48A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000463858
  gene symbol: BCL7B
  hgvsc: ENST00000463858.1:n.345-1893A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000106635
  ensembl protein: ENSP00000393230
  ensembl transcript: ENST00000411832
  gene symbol: BCL7B
  hgvsc: ENST00000411832.1:c.266-1893A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000482231
  gene symbol: BCL7B
  hgvsc: ENST00000482231.1:n.531A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000481667
  gene symbol: BCL7B
  hgvsc: ENST00000481667.1:n.493A>G
  variant of: http://identifiers.org/hgnc/1005
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000106635
  ensembl transcript: ENST00000493679
  gene symbol: BCL7B
  hgvsc: ENST00000493679.1:n.201A>G
  variant of: http://identifiers.org/hgnc/1005
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25700
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5419
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25050
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Thr138Ala
num of homozygotes: 0
reference allele: T

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29324
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2125
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6287
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3355
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3094
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 562
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1416
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9679
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4281
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511761504505049e-5
allele num: 66148
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10348
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.095e0

QD
type: SiteQuality
SIO_000300: 1.071e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.38e-1

FS
type: SiteQuality
SIO_000300: 1.233e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.8e-2

MQRankSum
type: SiteQuality
SIO_000300: -7.41e-1

DP
type: SiteQuality
SIO_000300: 1.892837e6

VQSLOD
type: SiteQuality
SIO_000300: 4.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.932e1

GenotypeDepth
all individuals: 125
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 569
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9638
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3082
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3347
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 90
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 677
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1417
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 39
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2123
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4268
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29269
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6285
bin: 9.75e1
variant carriers: 2

South Asian
type: Population
allele count: 2
allele frequency: 1.215214485356665e-4
allele num: 16458
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6522
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.890217e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.570000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.54e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.34e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.198e0

QD
type: SiteQuality
SIO_000300: 8.98e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

GenotypeDepth
all individuals: 30
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15710
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 78
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9605
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4258
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6282
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 162
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2123
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3346
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 750
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1416
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29149
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3079
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6504
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.029385034837928e-5
allele num: 66020
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10338
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16454
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.263e0

VQSLOD
type: SiteQuality
SIO_000300: 1.24e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 7.0e-3

QD
type: SiteQuality
SIO_000300: 1.194e1

MQ
type: SiteQuality
SIO_000300: 5.991e1

DP
type: SiteQuality
SIO_000300: 1.888551e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.378e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.89e-1

GenotypeDepth
all individuals: 268
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 569
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3340
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4250
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6277
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 24
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2123
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3076
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9607
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29144
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 786
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1415
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66004
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6496
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.077549532028686e-5
allele num: 16454
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.073e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.26e0

VQSLOD
type: SiteQuality
SIO_000300: 3.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 1.438e1

MQRankSum
type: SiteQuality
SIO_000300: 3.34e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.444e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.695e0

DP
type: SiteQuality
SIO_000300: 1.887861e6

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7209
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3316
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1412
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 46
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10318
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6442
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

Other
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allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65856
num of homozygotes: 0

South Asian
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allele frequency: 6.094588005850804e-5
allele num: 16408
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

MQRankSum
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SIO_000300: 5.52e-1

BaseQRankSum
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MQ
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SIO_000300: 6.0e1

ClippingRankSum
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FS
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InbreedingCoeff
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SIO_000300: -5.0e-4

QD
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ReadPosRankSum
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VQSLOD
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DP
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SIO_000300: 1.880847e6

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65862
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10318
num of homozygotes: 0

South Asian
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allele frequency: 6.098304671301378e-5
allele num: 16398
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
SIO_000300: 4.3e-2

FS
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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MQ
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InbreedingCoeff
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ClippingRankSum
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QD
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DP
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SIO_000300: 1.880938e6

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 1
allele frequency: 9.693679720822024e-5
allele num: 10316
num of homozygotes: 0

South Asian
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allele num: 16400
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Other
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
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East Asian
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

DP
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SIO_000300: 1.879996e6

MQ
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InbreedingCoeff
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QD
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VQSLOD
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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FS
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BaseQRankSum
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GenotypeDepth
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variant carriers: 3

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10316
num of homozygotes: 0

South Asian
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allele count: 7
allele frequency: 4.268292682926829e-4
allele num: 16400
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6436
num of homozygotes: 0

European (Non-Finnish)
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allele count: 7
allele frequency: 1.063118887066399e-4
allele num: 65844
num of homozygotes: 0

East Asian
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MQRankSum
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MQ
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VQSLOD
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FS
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DP
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InbreedingCoeff
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QD
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BaseQRankSum
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ClippingRankSum
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SIO_000300: 1.11e-1

ReadPosRankSum
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SIO_000300: -8.2e-2

GenotypeDepth
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65698
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11504
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
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FS
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DP
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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MQ
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InbreedingCoeff
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MQRankSum
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QD
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SIO_000300: 1.255e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10288
num of homozygotes: 0

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

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

South Asian
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allele frequency: 1.226091221186856e-4
allele num: 16312
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BaseQRankSum
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VQSLOD
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MQRankSum
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ClippingRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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QD
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DP
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MQ
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GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.051199121254653e-5
allele num: 65548
num of homozygotes: 0

European (Finnish)
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South Asian
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num of homozygotes: 0

African
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num of homozygotes: 0

East Asian
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Latino
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num of homozygotes: 0

Other
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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QD
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BaseQRankSum
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FS
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InbreedingCoeff
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VQSLOD
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MQ
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DP
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GenotypeDepth
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variant carriers: 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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 (Finnish)
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Latino
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Other
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European (Non-Finnish)
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East Asian
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ReadPosRankSum
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BaseQRankSum
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QD
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InbreedingCoeff
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MQ
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VQSLOD
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FS
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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East Asian
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European (Non-Finnish)
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African
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Other
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MQ
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FS
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DP
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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MQRankSum
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QD
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ReadPosRankSum
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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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Other
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European (Non-Finnish)
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Latino
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European (Finnish)
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African
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South Asian
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BaseQRankSum
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ReadPosRankSum
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FS
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InbreedingCoeff
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VQSLOD
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QD
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MQRankSum
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DP
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ClippingRankSum
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MQ
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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European (Non-Finnish)
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Other
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East Asian
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Latino
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MQ
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DP
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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QD
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FS
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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African
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South Asian
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Other
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Latino
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European (Finnish)
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BaseQRankSum
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InbreedingCoeff
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FS
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DP
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MQRankSum
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VQSLOD
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ReadPosRankSum
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MQ
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QD
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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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European (Non-Finnish)
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African
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South Asian
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Latino
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European (Finnish)
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East Asian
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MQRankSum
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QD
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MQ
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BaseQRankSum
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FS
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VQSLOD
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InbreedingCoeff
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DP
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ClippingRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Non-Finnish)
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African
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European (Finnish)
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East Asian
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South Asian
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QD
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VQSLOD
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MQRankSum
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FS
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DP
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 8.815232722143864e-5
allele num: 11344
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.13607426223853e-5
allele num: 63774
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African
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European (Finnish)
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allele frequency: 0.0e0
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Other
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MQ
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VQSLOD
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DP
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ClippingRankSum
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QD
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FS
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 11398
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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African
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Other
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South Asian
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European (Non-Finnish)
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allele num: 63756
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QD
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FS
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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MQRankSum
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DP
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MQ
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GenotypeDepth
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11416
num of homozygotes: 0

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

African
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
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allele num: 63864
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Other
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South Asian
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InbreedingCoeff
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FS
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MQRankSum
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DP
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VQSLOD
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QD
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ClippingRankSum
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BaseQRankSum
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MQ
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

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

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

European (Non-Finnish)
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allele num: 63736
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East Asian
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South Asian
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Latino
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Other
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InbreedingCoeff
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FS
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MQRankSum
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BaseQRankSum
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QD
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ReadPosRankSum
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MQ
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VQSLOD
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

Other
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African
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Latino
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European (Finnish)
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European (Non-Finnish)
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South Asian
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ReadPosRankSum
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FS
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MQ
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 7.603920243325448e-4
allele num: 11836
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European (Non-Finnish)
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East Asian
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Latino
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African
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European (Finnish)
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Other
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BaseQRankSum
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MQ
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QD
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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FS
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VQSLOD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

African
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European (Non-Finnish)
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allele count: 1
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allele num: 65000
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Other
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South Asian
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East Asian
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European (Finnish)
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FS
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VQSLOD
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DP
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InbreedingCoeff
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MQRankSum
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QD
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ClippingRankSum
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ReadPosRankSum
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MQ
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Finnish)
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African
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European (Non-Finnish)
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Other
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Latino
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ReadPosRankSum
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MQ
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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QD
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DP
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FS
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VQSLOD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Other
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African
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European (Finnish)
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Latino
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South Asian
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East Asian
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VQSLOD
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MQRankSum
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FS
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MQ
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InbreedingCoeff
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ClippingRankSum
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DP
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BaseQRankSum
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QD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 65280
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African
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European (Finnish)
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East Asian
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Other
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South Asian
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Latino
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InbreedingCoeff
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VQSLOD
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QD
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ReadPosRankSum
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MQ
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ClippingRankSum
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FS
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DP
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MQRankSum
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BaseQRankSum
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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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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 8

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 75
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.064347402992337e-4
allele num: 65768
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14020
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -4.305e0

FS
type: SiteQuality
SIO_000300: 6.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.2e-2

DP
type: SiteQuality
SIO_000300: 2.003129e6

MQRankSum
type: SiteQuality
SIO_000300: 2.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 7.8e-2

QD
type: SiteQuality
SIO_000300: 1.301e1

MQ
type: SiteQuality
SIO_000300: 5.916e1

VQSLOD
type: SiteQuality
SIO_000300: 1.55e0

GenotypeDepth
all individuals: 435
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7709
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 7.5e0
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
all individuals: 7
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15884
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65786
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14094
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.978e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.49e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.25e-1

QD
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SIO_000300: 1.269e1

DP
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SIO_000300: 2.003744e6

BaseQRankSum
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SIO_000300: 3.81e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

FS
type: SiteQuality
SIO_000300: 6.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 8.149999999999999e-1

GenotypeDepth
all individuals: 85
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 153
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variant carriers: 0

GenotypeQuality
all individuals: 3268
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1500
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GenotypeQuality
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GenotypeQuality
all individuals: 126
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 37
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GenotypeQuality
all individuals: 69
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.517911353976928e-5
allele num: 65880
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.86e0

BaseQRankSum
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SIO_000300: 3.92e0

DP
type: SiteQuality
SIO_000300: 2.008117e6

QD
type: SiteQuality
SIO_000300: 1.493e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.74e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.041e0

VQSLOD
type: SiteQuality
SIO_000300: 1.14e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.46e-1

GenotypeDepth
all individuals: 437
bin: 9.75e1
variant carriers: 2

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4284
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6569
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 10

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4797
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3458
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3268
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65952
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

South Asian
type: Population
allele count: 10
allele frequency: 6.812917291184085e-4
allele num: 14678
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.81e0

MQRankSum
type: SiteQuality
SIO_000300: 2.3e-1

QD
type: SiteQuality
SIO_000300: 1.291e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.21e0

FS
type: SiteQuality
SIO_000300: 1.354e0

MQ
type: SiteQuality
SIO_000300: 5.953e1

DP
type: SiteQuality
SIO_000300: 2.010686e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.19e-1

GenotypeDepth
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bin: 4.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 1047
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4
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GenotypeQuality
all individuals: 62
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GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 60
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GenotypeQuality
all individuals: 99
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GenotypeQuality
all individuals: 10
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
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GenotypeQuality
all individuals: 2241
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 4806
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GenotypeQuality
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GenotypeQuality
all individuals: 4287
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511990081345066e-5
allele num: 66138
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15210
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.018084e6

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

InbreedingCoeff
type: SiteQuality
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ClippingRankSum
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QD
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BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 7.65e-1

MQ
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SIO_000300: 5.961e1

MQRankSum
type: SiteQuality
SIO_000300: 5.28e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 6614
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 1
allele frequency: 1.123595505617978e-3
allele num: 890
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15244
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511304558094547e-5
allele num: 66168
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

DP
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SIO_000300: 2.018404e6

QD
type: SiteQuality
SIO_000300: 1.401e1

BaseQRankSum
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VQSLOD
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SIO_000300: 3.24e-1

MQRankSum
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SIO_000300: 4.64e-1

FS
type: SiteQuality
SIO_000300: 9.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.7e-1

MQ
type: SiteQuality
SIO_000300: 5.88e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.55e-1

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2239
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514325519413653e-5
allele num: 66036
num of homozygotes: 0

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

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

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

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

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

Other
type: Population
allele count: 0
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allele num: 886
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.8e-1

MQRankSum
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DP
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SIO_000300: 2.010448e6

MQ
type: SiteQuality
SIO_000300: 5.938e1

BaseQRankSum
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InbreedingCoeff
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SIO_000300: 4.0e-4

ClippingRankSum
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FS
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 2.277e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.78e-1

GenotypeDepth
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variant carriers: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.514600751241973e-5
allele num: 66024
num of homozygotes: 0

Other
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South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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VQSLOD
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ReadPosRankSum
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MQ
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SIO_000300: 5.94e1

BaseQRankSum
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SIO_000300: 1.63e0

MQRankSum
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DP
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FS
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 3.0e-4

ClippingRankSum
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QD
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SIO_000300: 3.082e1

GenotypeDepth
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variant carriers: 1

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

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

South Asian
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allele frequency: 2.048900423439421e-4
allele num: 14642
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 65894
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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Other
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VQSLOD
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SIO_000300: 8.54e-1

MQRankSum
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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QD
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FS
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MQ
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DP
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ReadPosRankSum
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SIO_000300: 1.25e0

GenotypeDepth
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65816
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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African
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South Asian
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allele num: 14474
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
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SIO_000300: 5.81e-1

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

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

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

Other
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South Asian
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allele frequency: 2.150229357798165e-4
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European (Finnish)
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European (Non-Finnish)
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East Asian
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Latino
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ReadPosRankSum
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MQRankSum
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DP
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ClippingRankSum
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FS
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VQSLOD
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MQ
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QD
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InbreedingCoeff
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BaseQRankSum
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GenotypeDepth
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variant carriers: 0

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

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

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

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

European (Finnish)
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num of homozygotes: 0

Other
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South Asian
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Latino
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East Asian
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European (Non-Finnish)
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African
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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DP
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InbreedingCoeff
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MQ
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FS
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QD
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GenotypeDepth
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variant carriers: 1

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

South Asian
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allele frequency: 7.6057195010648e-5
allele num: 13148
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.592633416000735e-5
allele num: 65322
num of homozygotes: 0

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

African
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allele 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: 8630
num of homozygotes: 0

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

ClippingRankSum
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SIO_000300: -4.66e-1

ReadPosRankSum
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SIO_000300: 3.07e-1

BaseQRankSum
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InbreedingCoeff
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VQSLOD
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FS
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MQRankSum
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SIO_000300: 1.3e-2

DP
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SIO_000300: 1.969942e6

MQ
type: SiteQuality
SIO_000300: 5.979e1

QD
type: SiteQuality
SIO_000300: 1.136e1

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65294
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10308
num of homozygotes: 0

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

Latino
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allele count: 1
allele frequency: 8.685079034219212e-5
allele num: 11514
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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Other
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MQRankSum
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SIO_000300: 8.120000000000001e-1

DP
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QD
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VQSLOD
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FS
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SIO_000300: 5.969e0

InbreedingCoeff
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ReadPosRankSum
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SIO_000300: 7.2e-1

MQ
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SIO_000300: 6.0e1

BaseQRankSum
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ClippingRankSum
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SIO_000300: -7.000000000000001e-2

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

African
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allele count: 1
allele frequency: 9.704968944099378e-5
allele num: 10304
num of homozygotes: 0

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

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

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

InbreedingCoeff
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VQSLOD
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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FS
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QD
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BaseQRankSum
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MQ
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SIO_000300: 6.0e1

DP
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SIO_000300: 1.967136e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10296
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65096
num of homozygotes: 0

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

Latino
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allele count: 1
allele frequency: 8.695652173913044e-5
allele num: 11500
num of homozygotes: 0

South Asian
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Other
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allele count: 0
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East Asian
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allele count: 0
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QD
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SIO_000300: 1.346e1

ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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DP
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SIO_000300: 1.961742e6

FS
type: SiteQuality
SIO_000300: 2.072e0

VQSLOD
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SIO_000300: -2.487e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

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

East Asian
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allele count: 1
allele frequency: 1.160900859066636e-4
allele num: 8614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65006
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African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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Other
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South Asian
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MQRankSum
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SIO_000300: 1.68e-1

MQ
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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DP
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ClippingRankSum
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FS
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SIO_000300: 1.913e0

ReadPosRankSum
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QD
type: SiteQuality
SIO_000300: 1.394e1

GenotypeDepth
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
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allele num: 64922
num of homozygotes: 0

Latino
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num of homozygotes: 0

South Asian
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allele num: 12196
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VQSLOD
type: SiteQuality
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FS
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MQRankSum
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ReadPosRankSum
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DP
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ClippingRankSum
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BaseQRankSum
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MQ
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QD
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InbreedingCoeff
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GenotypeDepth
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variant carriers: 0

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

African
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allele frequency: 0.0e0
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Other
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South Asian
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Latino
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East Asian
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European (Finnish)
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European (Non-Finnish)
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InbreedingCoeff
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VQSLOD
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DP
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MQRankSum
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ClippingRankSum
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FS
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ReadPosRankSum
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BaseQRankSum
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MQ
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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East Asian
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Latino
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South Asian
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European (Finnish)
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Other
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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MQ
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FS
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QD
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BaseQRankSum
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DP
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VQSLOD
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 8.721437292865864e-5
allele num: 11466
num of homozygotes: 0

Other
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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South Asian
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East Asian
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European (Finnish)
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VQSLOD
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QD
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ClippingRankSum
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InbreedingCoeff
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FS
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DP
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ReadPosRankSum
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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Other
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European (Finnish)
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East Asian
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Latino
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European (Non-Finnish)
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MQRankSum
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ReadPosRankSum
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QD
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DP
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BaseQRankSum
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MQ
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FS
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 6.490134994807892e-5
allele num: 15408
num of homozygotes: 0

Latino
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Other
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East Asian
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African
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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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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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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Other
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South Asian
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European (Finnish)
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East Asian
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European (Non-Finnish)
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InbreedingCoeff
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VQSLOD
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FS
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ReadPosRankSum
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DP
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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MQ
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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South Asian
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African
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Other
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European (Non-Finnish)
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allele num: 65330
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Latino
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FS
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MQRankSum
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QD
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VQSLOD
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MQ
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InbreedingCoeff
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ReadPosRankSum
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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European (Finnish)
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African
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European (Non-Finnish)
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Other
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South Asian
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VQSLOD
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InbreedingCoeff
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DP
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BaseQRankSum
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MQRankSum
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QD
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ReadPosRankSum
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FS
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MQ
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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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African
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MQRankSum
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MQ
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DP
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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South Asian
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European (Finnish)
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African
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East Asian
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VQSLOD
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MQ
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MQRankSum
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ReadPosRankSum
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FS
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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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African
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Latino
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East Asian
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European (Finnish)
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Other
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BaseQRankSum
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FS
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VQSLOD
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QD
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MQ
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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European (Finnish)
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European (Non-Finnish)
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African
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Other
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BaseQRankSum
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FS
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MQ
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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QD
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DP
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MQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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Latino
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East Asian
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FS
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VQSLOD
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QD
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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DP
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MQ
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GenotypeDepth
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GenotypeDepth
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East Asian
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South Asian
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European (Non-Finnish)
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Latino
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European (Finnish)
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African
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DP
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MQ
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ReadPosRankSum
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InbreedingCoeff
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FS
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VQSLOD
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