12-6760381-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760381
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760381
    reference: chr 12
allele count: 1
allele frequency: 8.241169586787756e-6
allele num: 121342
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.718C>T
  hgvsp: ENSP00000415903.2:p.Gln240Ter
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.*42C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.741C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*404C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*298C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.727C>T
  hgvsp: ENSP00000343396.4:p.Gln243Ter
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.730C>T
  hgvsp: ENSP00000380024.4:p.Gln244Ter
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*859C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.865C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.658C>T
  hgvsp: ENSP00000397343.2:p.Gln220Ter
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.721C>T
  hgvsp: ENSP00000412705.2:p.Gln241Ter
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.373C>T
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14037
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2928
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12194
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20807
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6115
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln244Ter
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

12-6760389-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760389
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760389
    reference: chr 12
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.*34G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.365G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.713G>A
  hgvsp: ENSP00000412705.2:p.Arg238His
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.710G>A
  hgvsp: ENSP00000415903.2:p.Arg237His
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.722G>A
  hgvsp: ENSP00000380024.4:p.Arg241His
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.733G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.650G>A
  hgvsp: ENSP00000397343.2:p.Arg217His
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.719G>A
  hgvsp: ENSP00000343396.4:p.Arg240His
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*396G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.857G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*851G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*290G>A
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2920
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6119
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14059
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12123
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20883
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg241His
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

12-6760405-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760405
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760405
    reference: chr 12
allele count: 2
allele frequency: 1.647962294622699e-5
allele num: 121362
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.702-5T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*279-5T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*385-5T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.699-5T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.354-5T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.711-5T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.*23-5T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.639-5T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*840-5T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.846-5T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.708-5T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.722-5T>C
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6110
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21006
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14054
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12041
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.711-5T>C
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP

12-6760412-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760412
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760412
    reference: chr 12
allele count: 3
allele frequency: 2.471780505891077e-5
allele num: 121370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.639-12T>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.722-12T>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*840-12T>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.711-12T>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.699-12T>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.*23-12T>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.702-12T>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.846-12T>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.354-12T>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.708-12T>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*279-12T>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*385-12T>A
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6111
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2920
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21038
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11999
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14063
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ

12-6760414-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760414
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760414
    reference: chr 12
allele count: 2
allele frequency: 1.647880825258717e-5
allele num: 121368
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.711-14C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.*23-14C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*279-14C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.722-14C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.846-14C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.702-14C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.708-14C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.699-14C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.639-14C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*840-14C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*385-14C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.354-14C>G
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6111
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21045
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11982
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2919
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14071
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

12-6760416-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760416
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760416
    reference: chr 12
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.702-16C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.711-16C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.639-16C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.354-16C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.846-16C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.*23-16C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*840-16C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*279-16C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*385-16C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.722-16C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.699-16C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.708-16C>T
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21047
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14076
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11980
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2919
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6113
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: DP

12-6760417-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760417
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760417
    reference: chr 12
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.354-17C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.702-17C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.846-17C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.711-17C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*385-17C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*840-17C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.639-17C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.*23-17C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*279-17C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.708-17C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.699-17C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.722-17C>G
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21042
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14082
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6109
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11982
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2919
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
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: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

12-6760421-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760421
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760420
    reference: chr 12
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*840-22delT
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*385-22delT
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.708-22delT
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.*23-22delT
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.846-22delT
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.702-22delT
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.711-22delT
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.722-22delT
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.639-22delT
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*279-22delT
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.699-22delT
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.354-22delT
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 6110
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2918
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21061
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14088
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: GA
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum

12-6760422-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760422
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760422
    reference: chr 12
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.722-22T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*385-22T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.699-22T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.702-22T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.*23-22T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.711-22T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*840-22T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.639-22T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.846-22T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*279-22T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.708-22T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.354-22T>C
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21066
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11972
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6108
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14084
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2916
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP

12-6760424-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760424
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760424
    reference: chr 12
allele count: 3
allele frequency: 2.471658317954126e-5
allele num: 121376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.708-24T>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.711-24T>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.846-24T>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.639-24T>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.722-24T>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*840-24T>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*279-24T>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.*23-24T>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.354-24T>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.699-24T>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.702-24T>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*385-24T>A
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2916
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6110
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14081
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11974
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

12-6760424-AAGTG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760424
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760420
    reference: chr 12
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.702-28_702-25delCACT
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.722-28_722-25delCACT
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*840-28_*840-25delCACT
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*279-28_*279-25delCACT
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.699-28_699-25delCACT
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.639-28_639-25delCACT
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.846-28_846-25delCACT
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.708-28_708-25delCACT
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.711-28_711-25delCACT
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*385-28_*385-25delCACT
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.*23-28_*23-25delCACT
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.354-28_354-25delCACT
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14081
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21074
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2916
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11974
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6110
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
reference allele: AAGTG
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

12-6760430-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760430
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760430
    reference: chr 12
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.354-30C>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*385-30C>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.708-30C>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.699-30C>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.*23-30C>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*279-30C>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*840-30C>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.722-30C>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.846-30C>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.702-30C>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.711-30C>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.639-30C>A
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2916
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11950
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6111
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14082
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD

http://identifiers.org/exac.variant/12-6760446-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760446
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760446
    reference: chr 12
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.*22+44G>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.638+44G>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*839+44G>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.845+44G>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*384+44G>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.721+44G>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.710+44G>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.353+44G>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.698+44G>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*278+44G>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.701+44G>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.707+44G>T
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14098
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21191
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6108
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2917
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11862
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

12-6760451-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760451
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760451
    reference: chr 12
allele count: 24
allele frequency: 1.977131182653969e-4
allele num: 121388
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.710+39T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.701+39T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.698+39T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.353+39T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.638+39T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.845+39T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*384+39T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.707+39T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.*22+39T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*839+39T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.721+39T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*278+39T>C
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6107
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11866
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14103
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21196
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

12-6760452-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760452
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760452
    reference: chr 12
allele count: 4
allele frequency: 3.295110056675893e-5
allele num: 121392
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.698+38G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.721+38G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.845+38G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.638+38G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.710+38G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*839+38G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.*22+38G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*384+38G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*278+38G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.701+38G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.353+38G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.707+38G>C
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11865
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14104
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6105
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21207
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD

12-6760470-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760470
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760470
    reference: chr 12
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.698+20G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*278+20G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.701+20G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.707+20G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.845+20G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.721+20G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.710+20G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.353+20G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*839+20G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.*22+20G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*384+20G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.638+20G>A
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6105
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2906
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14113
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11826
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21261
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

12-6760473-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760473
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760473
    reference: chr 12
allele count: 100
allele frequency: 8.237503706876668e-4
allele num: 121396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.698+17G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*839+17G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.353+17G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.707+17G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.*22+17G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*278+17G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.845+17G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.638+17G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.710+17G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*384+17G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.701+17G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.721+17G>C
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14101
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11801
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2909
  bin: 4.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 21239
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 6097
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

12-6760482-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760482
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760482
    reference: chr 12
allele count: 3
allele frequency: 2.471088267272907e-5
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.353+8G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.701+8G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*839+8G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*384+8G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*278+8G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.845+8G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.*22+8G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.710+8G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.638+8G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.707+8G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.721+8G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.698+8G>A
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2907
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6108
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14141
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21278
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.710+8G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

12-6760487-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760487
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760487
    reference: chr 12
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*384+3A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.638+3A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.845+3A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.721+3A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.710+3A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*278+3A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.*22+3A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.701+3A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*839+3A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.707+3A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.698+3A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.353+3A>G
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14141
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2905
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21291
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6104
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.710+3A>G
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

12-6760493-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760493
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760493
    reference: chr 12
allele count: 12
allele frequency: 9.884353069091628e-5
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*381A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.704A>G
  hgvsp: ENSP00000343396.4:p.Lys235Arg
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*275A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.*19A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.707A>G
  hgvsp: ENSP00000380024.4:p.Lys236Arg
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.350A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.695A>G
  hgvsp: ENSP00000415903.2:p.Lys232Arg
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.635A>G
  hgvsp: ENSP00000397343.2:p.Lys212Arg
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*836A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.698A>G
  hgvsp: ENSP00000412705.2:p.Lys233Arg
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.842A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.718A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.722A>G
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21295
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11800
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6102
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2907
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys236Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP

12-6760503-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760503
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760503
    reference: chr 12
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.694C>T
  hgvsp: ENSP00000343396.4:p.Pro232Ser
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.685C>T
  hgvsp: ENSP00000415903.2:p.Pro229Ser
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.688C>T
  hgvsp: ENSP00000412705.2:p.Pro230Ser
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.708C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.340C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.832C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.*9C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*826C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.625C>T
  hgvsp: ENSP00000397343.2:p.Pro209Ser
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*265C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.697C>T
  hgvsp: ENSP00000380024.4:p.Pro233Ser
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*371C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.712C>T
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11787
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14141
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21313
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6102
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2906
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro233Ser
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ

12-6760507-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760507
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760507
    reference: chr 12
allele count: 6
allele frequency: 4.942176534545814e-5
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.*5C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.690C>G
  hgvsp: ENST00000341550.4:c.690C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.708C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.828C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*367C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.693C>G
  hgvsp: ENST00000396807.4:c.693C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.621C>G
  hgvsp: ENST00000444704.2:c.621C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.681C>G
  hgvsp: ENST00000446105.2:c.681C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*261C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.684C>G
  hgvsp: ENST00000412586.2:c.684C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.336C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.704C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*822C>G
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21308
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2909
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6105
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14136
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11784
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr231Thr
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP

12-6760521-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760521
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760521
    reference: chr 12
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.679G>A
  hgvsp: ENSP00000380024.4:p.Val227Met
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.667G>A
  hgvsp: ENSP00000415903.2:p.Val223Met
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.322G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.676G>A
  hgvsp: ENSP00000343396.4:p.Val226Met
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.690G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*247G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*808G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.607G>A
  hgvsp: ENSP00000397343.2:p.Val203Met
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.531G>A
  hgvsp: ENST00000423703.2:c.531G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.694G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*353G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.670G>A
  hgvsp: ENSP00000412705.2:p.Val224Met
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.814G>A
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14143
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2903
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11766
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21319
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val227Met
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/12-6760522-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760522
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760522
    reference: chr 12
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*807T>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.675T>G
  hgvsp: ENSP00000343396.4:p.Cys225Trp
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.666T>G
  hgvsp: ENSP00000415903.2:p.Cys222Trp
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.606T>G
  hgvsp: ENSP00000397343.2:p.Cys202Trp
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.678T>G
  hgvsp: ENSP00000380024.4:p.Cys226Trp
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.813T>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.689T>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*246T>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.669T>G
  hgvsp: ENSP00000412705.2:p.Cys223Trp
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.530T>G
  hgvsp: ENSP00000414008.2:p.Val177Gly
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*352T>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.693T>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.321T>G
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21319
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6104
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11767
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14143
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2901
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys226Trp
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

12-6760531-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760531
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760531
    reference: chr 12
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*343T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*237T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.684T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.669T>C
  hgvsp: ENST00000396807.4:c.669T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.657T>C
  hgvsp: ENST00000446105.2:c.657T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*798T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.680T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.804T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.521T>C
  hgvsp: ENSP00000414008.2:p.Ile174Thr
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.597T>C
  hgvsp: ENST00000444704.2:c.597T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.153T>C
  hgvsp: ENST00000467678.1:c.153T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.666T>C
  hgvsp: ENST00000341550.4:c.666T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.660T>C
  hgvsp: ENST00000412586.2:c.660T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.312T>C
  variant of: http://identifiers.org/hgnc/19423
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11751
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6103
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21322
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2900
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile174Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ

12-6760546-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760546
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760546
    reference: chr 12
allele count: 5
allele frequency: 4.120381052839767e-5
allele num: 121348
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.665C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.138C>T
  hgvsp: ENST00000467678.1:c.138C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.642C>T
  hgvsp: ENST00000446105.2:c.642C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.789C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*783C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.651C>T
  hgvsp: ENST00000341550.4:c.651C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.645C>T
  hgvsp: ENST00000412586.2:c.645C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*222C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.506C>T
  hgvsp: ENSP00000414008.2:p.Pro169Leu
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*328C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.582C>T
  hgvsp: ENST00000444704.2:c.582C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.297C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.669C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.654C>T
  hgvsp: ENST00000396807.4:c.654C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11703
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14127
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21287
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro169Leu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD

12-6760554-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760554
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760554
    reference: chr 12
allele count: 19
allele frequency: 1.566390212534419e-4
allele num: 121298
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.133-3C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*778-3C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.292-3C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.577-3C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.660-3C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.664-3C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.640-3C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*323-3C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.649-3C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.784-3C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.501-3C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.646-3C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*217-3C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.637-3C>T
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14110
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2905
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11608
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.649-3C>T
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP

12-6760557-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760557
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760557
    reference: chr 12
allele count: 1
allele frequency: 8.244702778464837e-6
allele num: 121290
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.649-6T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.646-6T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.664-6T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.501-6T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.637-6T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.133-6T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.784-6T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.577-6T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.292-6T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*778-6T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*217-6T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.660-6T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*323-6T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.640-6T>C
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2900
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14085
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21138
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.649-6T>C
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP

12-6760569-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760569
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760569
    reference: chr 12
allele count: 4
allele frequency: 3.301038176506511e-5
allele num: 121174
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.640-18T>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*323-18T>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*778-18T>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.637-18T>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.660-18T>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.133-18T>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.577-18T>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.664-18T>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.784-18T>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.646-18T>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.649-18T>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.501-18T>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.292-18T>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*217-18T>A
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20680
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6066
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11178
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

12-6760571-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760571
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760571
    reference: chr 12
allele count: 4
allele frequency: 3.303055326176714e-5
allele num: 121100
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.649-20C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.640-20C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.784-20C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*217-20C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.664-20C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.501-20C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.646-20C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*323-20C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.292-20C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*778-20C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.577-20C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.660-20C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.637-20C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.133-20C>G
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2896
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10918
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13839
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/12-6760573-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760573
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760573
    reference: chr 12
allele count: 1
allele frequency: 8.259548037531387e-6
allele num: 121072
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.646-22T>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.664-22T>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*323-22T>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.577-22T>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.784-22T>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.501-22T>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.649-22T>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*778-22T>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.640-22T>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.660-22T>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.133-22T>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*217-22T>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.637-22T>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.292-22T>G
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6038
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13782
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10860
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD

12-6760575-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760575
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760574
    reference: chr 12
allele count: 1
allele frequency: 8.261458643138033e-6
allele num: 121044
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.133-25delG
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.637-25delG
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.501-25delG
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.649-25delG
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.640-25delG
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.646-25delG
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.577-25delG
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.292-25delG
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*778-25delG
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*217-25delG
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.660-25delG
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.664-25delG
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.784-25delG
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*323-25delG
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13679
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19979
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: TC
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP

12-6760576-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760576
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760576
    reference: chr 12
allele count: 9
allele frequency: 7.438385374481379e-5
allele num: 120994
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.649-25G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.133-25G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.637-25G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.660-25G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*323-25G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*217-25G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.784-25G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*778-25G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.664-25G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.646-25G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.577-25G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.640-25G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.292-25G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.501-25G>A
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13590
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19684
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6009
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2894
  bin: 4.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD

http://identifiers.org/exac.variant/12-6760576-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760576
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760575
    reference: chr 12
allele count: 7
allele frequency: 5.78541084681885e-5
allele num: 120994
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*323-26delT
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.292-26delT
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*778-26delT
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.577-26delT
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.501-26delT
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.660-26delT
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.649-26delT
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.784-26delT
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.640-26delT
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*217-26delT
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.637-26delT
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.646-26delT
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.133-26delT
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.664-26delT
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19684
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6009
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10394
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: CA
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

12-6760578-GGGGCCAGGAA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760578
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760568
    reference: chr 12
allele count: 1
allele frequency: 8.266239026567692e-6
allele num: 120974
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19586
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1755
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13503
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10277
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5993
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2078
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  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: Other
population: African
population: European (Finnish)
reference allele: GGGGCCAGGAA
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD

12-6760579-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760579
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760579
    reference: chr 12
allele count: 2
allele frequency: 1.654889370645572e-5
allele num: 120854
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.292-28C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.660-28C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.784-28C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*323-28C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.649-28C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.664-28C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.637-28C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.501-28C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*217-28C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.577-28C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.646-28C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*778-28C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.133-28C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.640-28C>T
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3000
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4610
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17950
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5861
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9014
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12734
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ

12-6760581-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760581
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760581
    reference: chr 12
allele count: 1
allele frequency: 8.274720728175424e-6
allele num: 120850
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*217-30C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*323-30C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*778-30C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.133-30C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.660-30C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.784-30C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.646-30C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.501-30C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.637-30C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.640-30C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.292-30C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.577-30C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.664-30C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.649-30C>T
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12476
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3015
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5738
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18172
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4602
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

12-6760586-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760586
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760586
    reference: chr 12
allele count: 11
allele frequency: 9.105809506465124e-5
allele num: 120802
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*778-35C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.292-35C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.784-35C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.501-35C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.664-35C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.133-35C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.640-35C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.660-35C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.577-35C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.649-35C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*323-35C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.637-35C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.646-35C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*217-35C>T
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9338
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5094
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11961
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18062
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3095
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

12-6760595-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760595
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760595
    reference: chr 12
allele count: 3
allele frequency: 2.494968480231533e-5
allele num: 120242
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.664-44C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*217-44C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*323-44C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.784-44C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*778-44C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.501-44C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.637-44C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.292-44C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.133-44C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.640-44C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.660-44C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.646-44C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.577-44C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.649-44C>T
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10190
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13821
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2805
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum

12-6760600-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760600
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760600
    reference: chr 12
allele count: 2
allele frequency: 1.669923016548937e-5
allele num: 119766
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*778-49T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.501-49T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.646-49T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.637-49T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.133-49T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.577-49T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.292-49T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.664-49T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.640-49T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*217-49T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.649-49T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.660-49T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*323-49T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.784-49T>C
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8168
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9277
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5371
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2791
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP

12-6760601-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6760601
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6760601
    reference: chr 12
allele count: 2
allele frequency: 1.671039219290477e-5
allele num: 119686
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*217-50C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.784-50C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.501-50C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.660-50C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.292-50C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.637-50C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.577-50C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.646-50C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*778-50C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.649-50C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.664-50C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.133-50C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*323-50C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.640-50C>T
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13879
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2793
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9231
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8175
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3221
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP

12-6761396-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6761396
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6761396
    reference: chr 12
allele count: 1
allele frequency: 8.528057308545113e-6
allele num: 117260
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.645+41C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.639+41C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.783+41C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*322+41C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.636+41C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*777+41C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.576+41C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.648+41C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*216+41C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.500+432C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.132+41C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.291+41C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.663+41C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.659+41C>T
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4731
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5889
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1761
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4454
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5226
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2283
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/12-6761399-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6761399
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6761399
    reference: chr 12
allele count: 1
allele frequency: 8.514261387824607e-6
allele num: 117450
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.500+429G>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.576+38G>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*322+38G>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.639+38G>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.659+38G>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.783+38G>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.648+38G>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*216+38G>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*777+38G>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.663+38G>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.132+38G>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.291+38G>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.645+38G>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.636+38G>T
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4732
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1713
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4454
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4504
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3566
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5846
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3402
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2090
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

12-6761400-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6761400
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6761400
    reference: chr 12
allele count: 1
allele frequency: 8.506439374606578e-6
allele num: 117558
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.663+37G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.576+37G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.639+37G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*777+37G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.648+37G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.500+428G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*216+37G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.132+37G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*322+37G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.645+37G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.783+37G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.659+37G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.636+37G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.291+37G>A
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3566
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2207
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2090
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2686
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2285
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4454
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

12-6761407-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6761407
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6761407
    reference: chr 12
allele count: 1
allele frequency: 8.498776176230622e-6
allele num: 117664
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.291+30G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.648+30G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.663+30G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*216+30G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.500+421G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.639+30G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*322+30G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.636+30G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.659+30G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.645+30G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.576+30G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*777+30G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.783+30G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.132+30G>A
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2090
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2016
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2296
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2686
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4502
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4731
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6180
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

12-6761409-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6761409
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6761409
    reference: chr 12
allele count: 1
allele frequency: 8.47802495930548e-6
allele num: 117952
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.639+28G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.500+419G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.636+28G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*322+28G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*777+28G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.132+28G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.783+28G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.663+28G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.576+28G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.645+28G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*216+28G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.659+28G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.648+28G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.291+28G>C
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6179
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2296
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3566
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1490
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4732
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5846
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2090
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

12-6761428-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6761428
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6761428
    reference: chr 12
allele count: 1
allele frequency: 8.37184381488179e-6
allele num: 119448
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.783+9C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.576+9C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.132+9C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.500+400C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*777+9C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.291+9C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.659+9C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*216+9C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.639+9C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.663+9C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.645+9C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.636+9C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.648+9C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*322+9C>T
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5226
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6179
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5846
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2318
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1743
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2686
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3417
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4730
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

12-6761437-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6761437
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6761437
    reference: chr 12
allele count: 64
allele frequency: 5.325168075617386e-4
allele num: 120184
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*216T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.639T>C
  hgvsp: ENST00000412586.2:c.639T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.645T>C
  hgvsp: ENST00000341550.4:c.645T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.132T>C
  hgvsp: ENST00000467678.1:c.132T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.663T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.783T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.659T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*322T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.576T>C
  hgvsp: ENST00000444704.2:c.576T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*777T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.648T>C
  hgvsp: ENST00000396807.4:c.648T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.636T>C
  hgvsp: ENST00000446105.2:c.636T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.291T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.500+391T>C
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5891
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3566
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.648T>C
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

12-6761442-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6761442
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6761442
    reference: chr 12
allele count: 1
allele frequency: 8.295726041943191e-6
allele num: 120544
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.654C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.658C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.631C>G
  hgvsp: ENSP00000415903.2:p.Pro211Ala
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.571C>G
  hgvsp: ENSP00000397343.2:p.Pro191Ala
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*317C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.643C>G
  hgvsp: ENSP00000380024.4:p.Pro215Ala
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.634C>G
  hgvsp: ENSP00000412705.2:p.Pro212Ala
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.640C>G
  hgvsp: ENSP00000343396.4:p.Pro214Ala
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.778C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.127C>G
  hgvsp: ENSP00000473635.1:p.Pro43Ala
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.286C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*211C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.500+386C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*772C>G
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4164
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6194
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2682
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2101
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2369
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5849
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro215Ala
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

12-6761445-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6761445
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6761445
    reference: chr 12
allele count: 1
allele frequency: 8.284866862189524e-6
allele num: 120702
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.568A>G
  hgvsp: ENSP00000397343.2:p.Asn190Asp
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.124A>G
  hgvsp: ENSP00000473635.1:p.Asn42Asp
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*769A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.775A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*314A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.655A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.628A>G
  hgvsp: ENSP00000415903.2:p.Asn210Asp
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.631A>G
  hgvsp: ENSP00000412705.2:p.Asn211Asp
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*208A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.651A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.283A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.500+383A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.640A>G
  hgvsp: ENSP00000380024.4:p.Asn214Asp
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.637A>G
  hgvsp: ENSP00000343396.4:p.Asn213Asp
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2367
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5892
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3565
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4735
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4453
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn214Asp
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

12-6761450-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6761450
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6761450
    reference: chr 12
allele count: 1
allele frequency: 8.271161767381846e-6
allele num: 120902
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.650G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.626G>A
  hgvsp: ENSP00000412705.2:p.Cys209Tyr
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.770G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.119G>A
  hgvsp: ENSP00000473635.1:p.Cys40Tyr
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*764G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*203G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.632G>A
  hgvsp: ENSP00000343396.4:p.Cys211Tyr
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*309G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.635G>A
  hgvsp: ENSP00000380024.4:p.Cys212Tyr
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.563G>A
  hgvsp: ENSP00000397343.2:p.Cys188Tyr
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.623G>A
  hgvsp: ENSP00000415903.2:p.Cys208Tyr
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.646G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.500+378G>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.278G>A
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4453
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2266
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2683
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5850
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4308
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys212Tyr
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: African
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP

12-6761471-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6761471
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6761471
    reference: chr 12
allele count: 1
allele frequency: 8.242935804015958e-6
allele num: 121316
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.749C>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.629C>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.611C>A
  hgvsp: ENSP00000343396.4:p.Ser204Tyr
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*288C>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.625C>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.542C>A
  hgvsp: ENSP00000397343.2:p.Ser181Tyr
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*182C>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.98C>A
  hgvsp: ENSP00000473635.1:p.Ser33Tyr
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*743C>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.614C>A
  hgvsp: ENSP00000380024.4:p.Ser205Tyr
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.500+357C>A
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.602C>A
  hgvsp: ENSP00000415903.2:p.Ser201Tyr
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.605C>A
  hgvsp: ENSP00000412705.2:p.Ser202Tyr
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.257C>A
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6194
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5892
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4735
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3565
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2089
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4398
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser205Tyr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

12-6761482-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6761482
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6761482
    reference: chr 12
allele count: 1
allele frequency: 8.239811473113496e-6
allele num: 121362
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*732T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.600T>C
  hgvsp: ENST00000341550.4:c.600T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.531T>C
  hgvsp: ENST00000444704.2:c.531T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*277T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.591T>C
  hgvsp: ENST00000446105.2:c.591T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.614T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.87T>C
  hgvsp: ENST00000467678.1:c.87T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.738T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.253-7T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*178-7T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.603T>C
  hgvsp: ENST00000396807.4:c.603T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.500+346T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.594T>C
  hgvsp: ENST00000412586.2:c.594T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.618T>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000436406
  ensembl transcript: ENST00000479301
  gene symbol: ING4
  hgvsc: ENST00000479301.1:c.*735T>C
  variant of: http://identifiers.org/hgnc/19423
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5849
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2089
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2411
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4411
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: n.253-7T>C
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD

12-6761503-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6761503
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6761503
    reference: chr 12
allele count: 5
allele frequency: 4.119091163725636e-5
allele num: 121386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.570C>T
  hgvsp: ENST00000446105.2:c.570C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.510C>T
  hgvsp: ENST00000444704.2:c.510C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.717C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*178-28C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.579C>T
  hgvsp: ENST00000341550.4:c.579C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000436406
  ensembl transcript: ENST00000479301
  gene symbol: ING4
  hgvsc: ENST00000479301.1:c.*714C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.597C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*711C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.573C>T
  hgvsp: ENST00000412586.2:c.573C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.593C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.582C>T
  hgvsp: ENST00000396807.4:c.582C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.66C>T
  hgvsp: ENST00000467678.1:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.500+325C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*256C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.253-28C>T
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5847
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2089
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4454
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5893
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2682
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3565
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn194Asn
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

12-6761504-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6761504
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6761504
    reference: chr 12
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.596A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.592A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*255A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*178-29A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.65A>G
  hgvsp: ENSP00000473635.1:p.Asn22Ser
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.569A>G
  hgvsp: ENSP00000415903.2:p.Asn190Ser
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.581A>G
  hgvsp: ENSP00000380024.4:p.Asn194Ser
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.572A>G
  hgvsp: ENSP00000412705.2:p.Asn191Ser
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.509A>G
  hgvsp: ENSP00000397343.2:p.Asn170Ser
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.716A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*710A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.253-29A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.500+324A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000436406
  ensembl transcript: ENST00000479301
  gene symbol: ING4
  hgvsc: ENST00000479301.1:c.*713A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.578A>G
  hgvsp: ENSP00000343396.4:p.Asn193Ser
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2682
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2584
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4736
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2089
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4453
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4425
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn194Ser
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
reference allele: T
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ

12-6761539-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6761539
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6761539
    reference: chr 12
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*220C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.30C>T
  hgvsp: ENST00000467678.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*675C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.543C>T
  hgvsp: ENST00000341550.4:c.543C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000436406
  ensembl transcript: ENST00000479301
  gene symbol: ING4
  hgvsc: ENST00000479301.1:c.*678C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.557C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.537C>T
  hgvsp: ENST00000412586.2:c.537C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.534C>T
  hgvsp: ENST00000446105.2:c.534C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.253-64C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000437198
  ensembl transcript: ENST00000493873
  gene symbol: ING4
  hgvsc: ENST00000493873.1:c.30C>T
  hgvsp: ENST00000493873.1:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.546C>T
  hgvsp: ENST00000396807.4:c.546C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.474C>T
  hgvsp: ENST00000444704.2:c.474C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.561C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.681C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.500+289C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*178-64C>T
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4404
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2584
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2682
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6197
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2089
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3565
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His182His
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ

12-6761563-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6761563
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6761563
    reference: chr 12
allele count: 68
allele frequency: 5.608247422680412e-4
allele num: 121250
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.519C>T
  hgvsp: ENST00000341550.4:c.519C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*651C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.450C>T
  hgvsp: ENST00000444704.2:c.450C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.533C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.253-88C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.500+265C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.537C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.657C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.510C>T
  hgvsp: ENST00000446105.2:c.510C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.513C>T
  hgvsp: ENST00000412586.2:c.513C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*196C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000436406
  ensembl transcript: ENST00000479301
  gene symbol: ING4
  hgvsc: ENST00000479301.1:c.*654C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.522C>T
  hgvsp: ENST00000396807.4:c.522C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*178-88C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000437198
  ensembl transcript: ENST00000493873
  gene symbol: ING4
  hgvsc: ENST00000493873.1:c.6C>T
  hgvsp: ENST00000493873.1:c.6C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.6C>T
  hgvsp: ENST00000467678.1:c.6C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4451
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2677
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5892
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4735
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5227
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro174Pro
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum

12-6761566-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6761566
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6761566
    reference: chr 12
allele count: 1
allele frequency: 8.249736008447729e-6
allele num: 121216
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.530G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.253-91G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.507G>C
  hgvsp: ENSP00000415903.2:p.Met169Ile
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.500+262G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*193G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.534G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000437198
  ensembl transcript: ENST00000493873
  gene symbol: ING4
  hgvsc: ENST00000493873.1:c.3G>C
  hgvsp: ENSP00000437198.1:p.Met1?
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.3G>C
  hgvsp: ENSP00000473635.1:p.Met1?
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.519G>C
  hgvsp: ENSP00000380024.4:p.Met173Ile
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*178-91G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*648G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.447G>C
  hgvsp: ENSP00000397343.2:p.Met149Ile
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.654G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.516G>C
  hgvsp: ENSP00000343396.4:p.Met172Ile
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000436406
  ensembl transcript: ENST00000479301
  gene symbol: ING4
  hgvsc: ENST00000479301.1:c.*651G>C
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.510G>C
  hgvsp: ENSP00000412705.2:p.Met170Ile
  variant of: http://identifiers.org/hgnc/19423
canonical: false
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2548
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4430
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4743
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5855
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2396
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met1?
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/12-6761569-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6761569
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6761569
    reference: chr 12
allele count: 1
allele frequency: 8.253140319891718e-6
allele num: 121166
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.507G>T
  hgvsp: ENST00000412586.2:c.507G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*645G>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.527G>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.651G>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000436406
  ensembl transcript: ENST00000479301
  gene symbol: ING4
  hgvsc: ENST00000479301.1:c.*648G>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*190G>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*178-94G>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.500+259G>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.-1G>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.444G>T
  hgvsp: ENST00000444704.2:c.444G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.504G>T
  hgvsp: ENST00000446105.2:c.504G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.516G>T
  hgvsp: ENST00000396807.4:c.516G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.513G>T
  hgvsp: ENST00000341550.4:c.513G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.531G>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000437198
  ensembl transcript: ENST00000493873
  gene symbol: ING4
  hgvsc: ENST00000493873.1:c.-1G>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.253-94G>T
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4741
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3570
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly172Gly
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD

12-6761579-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6761579
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6761579
    reference: chr 12
allele count: 1
allele frequency: 8.265009256810368e-6
allele num: 120992
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.506C>G
  hgvsp: ENSP00000380024.4:p.Pro169Arg
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.497C>G
  hgvsp: ENSP00000412705.2:p.Pro166Arg
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.-11C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.253-104C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000436406
  ensembl transcript: ENST00000479301
  gene symbol: ING4
  hgvsc: ENST00000479301.1:c.*638C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.517C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.521C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*178-104C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.503C>G
  hgvsp: ENSP00000343396.4:p.Pro168Arg
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.641C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.494C>G
  hgvsp: ENSP00000415903.2:p.Pro165Arg
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*635C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.500+249C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000437198
  ensembl transcript: ENST00000493873
  gene symbol: ING4
  hgvsc: ENST00000493873.1:c.-11C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*180C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.434C>G
  hgvsp: ENSP00000397343.2:p.Pro145Arg
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2087
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3570
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6205
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5903
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro169Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

12-6761580-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6761580
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6761580
    reference: chr 12
allele count: 3
allele frequency: 2.479707725116133e-5
allele num: 120982
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.500+248C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*634C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.516C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.493C>G
  hgvsp: ENSP00000415903.2:p.Pro165Ala
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.496C>G
  hgvsp: ENSP00000412705.2:p.Pro166Ala
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.433C>G
  hgvsp: ENSP00000397343.2:p.Pro145Ala
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000436406
  ensembl transcript: ENST00000479301
  gene symbol: ING4
  hgvsc: ENST00000479301.1:c.*637C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000437198
  ensembl transcript: ENST00000493873
  gene symbol: ING4
  hgvsc: ENST00000493873.1:c.-12C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.505C>G
  hgvsp: ENSP00000380024.4:p.Pro169Ala
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.640C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.502C>G
  hgvsp: ENSP00000343396.4:p.Pro168Ala
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.520C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.-12C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*179C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*178-105C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.253-105C>G
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4457
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2086
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5855
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3799
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4431
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Pro169Ala
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/12-6761581-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6761581
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6761581
    reference: chr 12
allele count: 1
allele frequency: 8.26801600687899e-6
allele num: 120948
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.504T>G
  hgvsp: ENSP00000380024.4:p.Ser168Arg
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.492T>G
  hgvsp: ENSP00000415903.2:p.Ser164Arg
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.500+247T>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.495T>G
  hgvsp: ENSP00000412705.2:p.Ser165Arg
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.432T>G
  hgvsp: ENSP00000397343.2:p.Ser144Arg
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*178T>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000436406
  ensembl transcript: ENST00000479301
  gene symbol: ING4
  hgvsc: ENST00000479301.1:c.*636T>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.515T>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*633T>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.-13T>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.501T>G
  hgvsp: ENSP00000343396.4:p.Ser167Arg
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.253-106T>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.639T>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.519T>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*178-106T>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000437198
  ensembl transcript: ENST00000493873
  gene symbol: ING4
  hgvsc: ENST00000493873.1:c.-13T>G
  variant of: http://identifiers.org/hgnc/19423
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6205
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4457
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2365
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3743
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser168Arg
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD

12-6761598-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6761598
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6761598
    reference: chr 12
allele count: 1
allele frequency: 8.29531314807134e-6
allele num: 120550
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*175-14C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.622C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000437198
  ensembl transcript: ENST00000493873
  gene symbol: ING4
  hgvsc: ENST00000493873.1:c.-16-14C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.-16-14C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000436406
  ensembl transcript: ENST00000479301
  gene symbol: ING4
  hgvsc: ENST00000479301.1:c.*633-14C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.500+230C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.492-14C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*178-123C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.429-14C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.512-14C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.498-14C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.253-123C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.501-14C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.489-14C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.516-14C>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*630-14C>G
  variant of: http://identifiers.org/hgnc/19423
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2086
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6205
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5905
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2830
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2306
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2027
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4739
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

12-6761608-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6761608
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6761608
    reference: chr 12
allele count: 2
allele frequency: 1.661792076575379e-5
allele num: 120352
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.489-24C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.253-133C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.429-24C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.-16-24C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.500+220C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000437198
  ensembl transcript: ENST00000493873
  gene symbol: ING4
  hgvsc: ENST00000493873.1:c.-16-24C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*178-133C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*630-24C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.612C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*175-24C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.492-24C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.501-24C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.516-24C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000436406
  ensembl transcript: ENST00000479301
  gene symbol: ING4
  hgvsc: ENST00000479301.1:c.*633-24C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.512-24C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.498-24C>T
  variant of: http://identifiers.org/hgnc/19423
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2086
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1759
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5905
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2678
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2285
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff

12-6761610-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6761610
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6761610
    reference: chr 12
allele count: 1
allele frequency: 8.313104778372627e-6
allele num: 120292
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000433081
  ensembl transcript: ENST00000469749
  gene symbol: ING4
  hgvsc: ENST00000469749.1:c.*175-26C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000431892
  ensembl transcript: ENST00000488381
  gene symbol: ING4
  hgvsc: ENST00000488381.1:c.*630-26C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000437149
  gene symbol: ING4
  hgvsc: ENST00000437149.2:n.516-26C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.489-26C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000472002
  gene symbol: ING4
  hgvsc: ENST00000472002.1:n.512-26C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.429-26C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000484795
  gene symbol: ING4
  hgvsc: ENST00000484795.1:n.610C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000412705
  ensembl transcript: ENST00000412586
  gene symbol: ING4
  hgvsc: ENST00000412586.2:c.492-26C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.498-26C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000437198
  ensembl transcript: ENST00000493873
  gene symbol: ING4
  hgvsc: ENST00000493873.1:c.-16-26C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.-16-26C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*178-135C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.501-26C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl transcript: ENST00000486287
  gene symbol: ING4
  hgvsc: ENST00000486287.1:n.253-135C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000436406
  ensembl transcript: ENST00000479301
  gene symbol: ING4
  hgvsc: ENST00000479301.1:c.*633-26C>T
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.500+218C>T
  variant of: http://identifiers.org/hgnc/19423
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4739
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6206
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2276
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2029
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

12-6761616-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6761616
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 6761616
    reference: chr 12
allele count: 3
allele frequency: 2.497627254108597e-5
allele num: 120114
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000414008
  ensembl transcript: ENST00000423703
  gene symbol: ING4
  hgvsc: ENST00000423703.2:c.500+212A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000437198
  ensembl transcript: ENST00000493873
  gene symbol: ING4
  hgvsc: ENST00000493873.1:c.-16-32A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000380024
  ensembl transcript: ENST00000396807
  gene symbol: ING4
  hgvsc: ENST00000396807.4:c.501-32A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000436406
  ensembl transcript: ENST00000479301
  gene symbol: ING4
  hgvsc: ENST00000479301.1:c.*633-32A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000343396
  ensembl transcript: ENST00000341550
  gene symbol: ING4
  hgvsc: ENST00000341550.4:c.498-32A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000397343
  ensembl transcript: ENST00000444704
  gene symbol: ING4
  hgvsc: ENST00000444704.2:c.429-32A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000473635
  ensembl transcript: ENST00000467678
  gene symbol: ING4
  hgvsc: ENST00000467678.1:c.-16-32A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000415903
  ensembl transcript: ENST00000446105
  gene symbol: ING4
  hgvsc: ENST00000446105.2:c.489-32A>G
  variant of: http://identifiers.org/hgnc/19423
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000111653
  ensembl protein: ENSP00000435867
  ensembl transcript: ENST00000482489
  gene symbol: ING4
  hgvsc: ENST00000482489.1:c.*178-141A>G
  variant of: http://identifiers.org/hgnc/19423
canonical: false
consequence: non coding transcript exon
filter: PASS
num of homozygotes: 0
reference allele: T

GenotypeDepth
all individuals: 1467
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 123
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 122
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27588
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10242
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3915
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3385
bin: 8.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 50
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6946
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4826
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2041
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1485
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 8.22e-1

QD
type: SiteQuality
SIO_000300: 1.265e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.961e1

FS
type: SiteQuality
SIO_000300: 5.427e0

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.75e-1

DP
type: SiteQuality
SIO_000300: 1.909956e6

GenotypeDepth
all individuals: 784
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1467
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 123
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4833
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 41
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27595
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2041
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10240
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6945
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1483
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3384
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3915
bin: 7.25e1
variant carriers: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 1.910559e6

MQRankSum
type: SiteQuality
SIO_000300: 4.32e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.092e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.505e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.653e0

FS
type: SiteQuality
SIO_000300: 1.378e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 5.81e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

GenotypeDepth
all individuals: 2921
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 357
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 295
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 527
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 76
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3919
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4809
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2036
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27703
bin: 6.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 3373
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10264
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 42
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6937
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1482
bin: 8.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.659508139937652e-5
allele num: 11548
num of homozygotes: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.3e0

VQSLOD
type: SiteQuality
SIO_000300: 3.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.92e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.16e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.506e0

QD
type: SiteQuality
SIO_000300: 1.322e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.45e0

DP
type: SiteQuality
SIO_000300: 1.91123e6

GenotypeDepth
all individuals: 157
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 122
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4809
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1481
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 53
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3918
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 27681
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6936
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3377
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2036
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10255
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 3
allele frequency: 2.596952908587258e-4
allele num: 11552
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
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: 66732
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -7.062e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.981e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.0108e1

MQRankSum
type: SiteQuality
SIO_000300: 3.12e-1

QD
type: SiteQuality
SIO_000300: 1.13e1

DP
type: SiteQuality
SIO_000300: 1.911627e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 780
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 122
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6934
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3920
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2036
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4803
bin: 7.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 27695
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1478
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 47
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10248
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3373
bin: 8.25e1
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Latino
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European (Finnish)
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European (Non-Finnish)
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East Asian
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African
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South Asian
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FS
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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QD
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MQ
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InbreedingCoeff
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MQRankSum
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DP
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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African
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South Asian
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Latino
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European (Non-Finnish)
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FS
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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QD
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MQ
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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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European (Non-Finnish)
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African
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Latino
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Other
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European (Finnish)
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DP
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MQ
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ReadPosRankSum
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FS
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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VQSLOD
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BaseQRankSum
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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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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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European (Finnish)
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South Asian
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European (Non-Finnish)
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East Asian
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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FS
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DP
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ReadPosRankSum
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MQ
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QD
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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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Other
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South Asian
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European (Non-Finnish)
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European (Finnish)
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African
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East Asian
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ReadPosRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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QD
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FS
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BaseQRankSum
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ClippingRankSum
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MQ
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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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Latino
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African
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European (Finnish)
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South Asian
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East Asian
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European (Non-Finnish)
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Other
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InbreedingCoeff
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FS
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QD
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VQSLOD
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DP
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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South Asian
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East Asian
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African
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Latino
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VQSLOD
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MQ
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FS
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QD
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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Other
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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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ClippingRankSum
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SIO_000300: -1.683e0

VQSLOD
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DP
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InbreedingCoeff
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MQRankSum
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MQ
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ReadPosRankSum
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BaseQRankSum
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FS
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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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GenotypeQuality
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variant carriers: 0

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

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

Latino
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FS
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InbreedingCoeff
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MQ
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QD
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MQRankSum
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ReadPosRankSum
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DP
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ClippingRankSum
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VQSLOD
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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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variant carriers: 24

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele num: 10404
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South Asian
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Other
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European (Non-Finnish)
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European (Finnish)
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East Asian
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ReadPosRankSum
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SIO_000300: 4.95e-1

DP
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MQ
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VQSLOD
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FS
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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QD
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BaseQRankSum
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GenotypeDepth
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variant carriers: 2

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: 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

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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num of homozygotes: 0

European (Non-Finnish)
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num of homozygotes: 0

Other
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East Asian
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allele num: 8654
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InbreedingCoeff
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SIO_000300: -1.0e-4

FS
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SIO_000300: 3.362e0

BaseQRankSum
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ClippingRankSum
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MQRankSum
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MQ
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VQSLOD
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DP
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ReadPosRankSum
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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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GenotypeQuality
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variant carriers: 0

Latino
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allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

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

South Asian
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East Asian
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African
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Latino
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European (Non-Finnish)
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MQ
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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FS
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VQSLOD
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MQRankSum
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InbreedingCoeff
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QD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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South Asian
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European (Finnish)
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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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BaseQRankSum
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ReadPosRankSum
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FS
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InbreedingCoeff
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ClippingRankSum
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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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South Asian
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Other
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African
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allele frequency: 0.0e0
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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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Latino
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allele num: 11576
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East Asian
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QD
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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MQRankSum
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DP
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FS
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BaseQRankSum
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InbreedingCoeff
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MQ
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SIO_000300: 6.0e1

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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bin: 9.75e1
variant carriers: 12

European (Non-Finnish)
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allele count: 12
allele frequency: 1.798183834327329e-4
allele num: 66734
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

South Asian
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num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
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DP
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ReadPosRankSum
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BaseQRankSum
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QD
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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MQRankSum
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FS
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MQ
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SIO_000300: 5.947e1

GenotypeDepth
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variant carriers: 1

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

South Asian
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allele count: 5
allele frequency: 3.028100775193798e-4
allele num: 16512
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

African
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allele count: 0
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

European (Non-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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ClippingRankSum
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MQ
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BaseQRankSum
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MQRankSum
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VQSLOD
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QD
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InbreedingCoeff
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FS
type: SiteQuality
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ReadPosRankSum
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SIO_000300: 4.33e-1

DP
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SIO_000300: 1.912825e6

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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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 7.495128166691651e-5
allele num: 66710
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East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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Other
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MQRankSum
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BaseQRankSum
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MQ
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VQSLOD
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DP
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InbreedingCoeff
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ReadPosRankSum
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FS
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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South Asian
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African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 10
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European (Non-Finnish)
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num of homozygotes: 0

Other
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QD
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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MQ
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FS
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InbreedingCoeff
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

European (Finnish)
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allele frequency: 0.0e0
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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QD
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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FS
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MQ
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DP
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GenotypeDepth
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variant carriers: 2

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

European (Non-Finnish)
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allele frequency: 3.002822653294096e-5
allele num: 66604
num of homozygotes: 0

East Asian
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South Asian
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allele num: 16494
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European (Finnish)
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African
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Latino
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Other
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ReadPosRankSum
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MQ
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FS
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ClippingRankSum
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DP
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VQSLOD
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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QD
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Non-Finnish)
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East Asian
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European (Finnish)
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South Asian
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Other
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FS
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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DP
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MQ
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MQRankSum
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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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Latino
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European (Non-Finnish)
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Other
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European (Finnish)
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African
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South Asian
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East Asian
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DP
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BaseQRankSum
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QD
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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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VQSLOD
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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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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 9819
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502900598154438e-5
allele num: 66538
num of homozygotes: 0

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.73e0

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

QD
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SIO_000300: 1.714e1

ClippingRankSum
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SIO_000300: -6.28e-1

MQ
type: SiteQuality
SIO_000300: 5.938e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.48e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.87426e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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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: 1.75e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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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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GenotypeQuality
all individuals: 6874
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variant carriers: 9

GenotypeQuality
all individuals: 3789
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 9
allele frequency: 8.677207867335133e-4
allele num: 10372
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66502
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.7e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.92e-1

QD
type: SiteQuality
SIO_000300: 1.365e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
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SIO_000300: 2.37e-1

BaseQRankSum
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SIO_000300: -3.479e0

DP
type: SiteQuality
SIO_000300: 1.867229e6

VQSLOD
type: SiteQuality
SIO_000300: 5.42e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
all individuals: 2014
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3309
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variant carriers: 0

GenotypeQuality
all individuals: 6874
bin: 9.75e1
variant carriers: 7

Latino
type: Population
allele count: 7
allele frequency: 6.071118820468344e-4
allele num: 11530
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66502
num of homozygotes: 0

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.867229e6

QD
type: SiteQuality
SIO_000300: 1.365e1

VQSLOD
type: SiteQuality
SIO_000300: 5.42e0

MQRankSum
type: SiteQuality
SIO_000300: 6.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.92e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.479e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.37e-1

GenotypeDepth
all individuals: 124
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
all individuals: 347
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 9
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 195
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GenotypeQuality
all individuals: 4652
bin: 7.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.685079034219212e-5
allele num: 11514
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: 66502
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 5.0e-1

MQ
type: SiteQuality
SIO_000300: 5.37e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.92e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.84e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

FS
type: SiteQuality
SIO_000300: 6.384e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.501e0

DP
type: SiteQuality
SIO_000300: 1.863054e6

QD
type: SiteQuality
SIO_000300: 4.98e0

GenotypeDepth
all individuals: 124
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variant carriers: 0

GenotypeDepth
all individuals: 767
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
all individuals: 292
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GenotypeDepth
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GenotypeQuality
all individuals: 724
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 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
all individuals: 25
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1980
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GenotypeQuality
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variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 1.93050193050193e-4
allele num: 10360
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66424
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.297e0

InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.616e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.18e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.92e-1

QD
type: SiteQuality
SIO_000300: 1.351e1

MQ
type: SiteQuality
SIO_000300: 5.936e1

GenotypeDepth
all individuals: 124
bin: 8.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 727
bin: 4.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66442
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.66183574879227e-5
allele num: 10350
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 4.544e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.68e-1

MQ
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SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: -2.829e0

MQRankSum
type: SiteQuality
SIO_000300: -4.78e-1

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 4.64e-1

GenotypeDepth
all individuals: 124
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variant carriers: 0

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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variant carriers: 0

GenotypeQuality
all individuals: 1969
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variant carriers: 0

GenotypeQuality
all individuals: 22358
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16444
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.656327169788592e-4
allele num: 66412
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.506e1

InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 1.31e0

MQRankSum
type: SiteQuality
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ClippingRankSum
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SIO_000300: -5.43e-1

MQ
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6592
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 4.540226405956777e-5
allele num: 66076
num of homozygotes: 0

South Asian
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BaseQRankSum
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MQ
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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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QD
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DP
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ClippingRankSum
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GenotypeDepth
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variant carriers: 0

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

European (Finnish)
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allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 3.039421294185587e-5
allele num: 65802
num of homozygotes: 0

African
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allele count: 0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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BaseQRankSum
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SIO_000300: 3.58e0

MQ
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ReadPosRankSum
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VQSLOD
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QD
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InbreedingCoeff
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MQRankSum
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FS
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SIO_000300: 0.0e0

ClippingRankSum
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DP
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 0.0e0
allele num: 65780
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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 1.948558067030398e-4
allele num: 10264
num of homozygotes: 0

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

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

Other
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MQRankSum
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SIO_000300: 2.89e-1

ReadPosRankSum
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QD
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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MQ
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SIO_000300: 6.0e1

FS
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InbreedingCoeff
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DP
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GenotypeDepth
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variant carriers: 0

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

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

Other
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Latino
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num of homozygotes: 0

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

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

European (Finnish)
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num of homozygotes: 0

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

Latino
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South Asian
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East Asian
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Other
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African
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European (Finnish)
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InbreedingCoeff
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MQ
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MQRankSum
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FS
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DP
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ReadPosRankSum
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VQSLOD
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QD
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BaseQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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European (Finnish)
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South Asian
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European (Non-Finnish)
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Latino
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QD
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InbreedingCoeff
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FS
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DP
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BaseQRankSum
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VQSLOD
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MQ
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ClippingRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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European (Finnish)
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European (Non-Finnish)
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African
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Other
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VQSLOD
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InbreedingCoeff
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QD
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ClippingRankSum
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DP
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FS
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MQ
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Non-Finnish)
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Latino
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European (Finnish)
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Other
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South Asian
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ClippingRankSum
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MQ
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VQSLOD
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QD
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FS
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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DP
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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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East Asian
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South Asian
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African
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Latino
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Other
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European (Finnish)
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European (Non-Finnish)
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ClippingRankSum
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InbreedingCoeff
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DP
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FS
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BaseQRankSum
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MQRankSum
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VQSLOD
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QD
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MQ
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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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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East Asian
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Other
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Latino
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European (Non-Finnish)
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QD
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ClippingRankSum
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ReadPosRankSum
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FS
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MQRankSum
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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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Other
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European (Non-Finnish)
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African
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MQ
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QD
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InbreedingCoeff
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VQSLOD
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FS
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DP
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GenotypeQuality
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European (Finnish)
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African
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European (Non-Finnish)
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South Asian
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MQ
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QD
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FS
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VQSLOD
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MQRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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Latino
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East Asian
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African
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South Asian
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BaseQRankSum
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MQ
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ReadPosRankSum
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DP
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MQRankSum
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InbreedingCoeff
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FS
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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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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DP
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MQ
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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South Asian
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European (Non-Finnish)
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allele frequency: 9.601248162261094e-4
allele num: 66658
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Latino
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allele frequency: 1.727712508638562e-4
allele num: 11576
num of homozygotes: 0

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

European (Finnish)
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African
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Other
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East Asian
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South Asian
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European (Non-Finnish)
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InbreedingCoeff
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MQRankSum
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FS
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DP
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ReadPosRankSum
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QD
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ClippingRankSum
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MQ
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BaseQRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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Latino
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European (Finnish)
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Other
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East Asian
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African
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VQSLOD
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MQ
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QD
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DP
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BaseQRankSum
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InbreedingCoeff
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FS
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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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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African
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South Asian
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Other
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Latino
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European (Non-Finnish)
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European (Finnish)
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East Asian
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MQ
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VQSLOD
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QD
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ReadPosRankSum
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FS
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DP
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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GenotypeQuality
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Latino
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African
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European (Non-Finnish)
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European (Finnish)
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East Asian
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South Asian
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DP
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ClippingRankSum
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MQ
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
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QD
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1905
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46277
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1011
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.620935154897056e-5
allele num: 10394
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15978
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66452
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.4e0

FS
type: SiteQuality
SIO_000300: 7.21e-1

DP
type: SiteQuality
SIO_000300: 3.514531e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.91e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

QD
type: SiteQuality
SIO_000300: 1.6e1

MQRankSum
type: SiteQuality
SIO_000300: -4.69e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.202e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.0e-2

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

GenotypeDepth
all individuals: 463
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1526
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3392
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5855
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6206
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4429
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4739
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4457
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1005
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3569
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1010
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 748
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 677
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1128
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1326
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1905
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 528
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3419
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1450
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1218
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46277
bin: 9.75e1
variant carriers: 2

South Asian
type: Population
allele count: 1
allele frequency: 6.304375236414071e-5
allele num: 15862
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66378
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

QD
type: SiteQuality
SIO_000300: 1.26e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.330000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.85e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.91e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.39e0

DP
type: SiteQuality
SIO_000300: 3.504003e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

GenotypeDepth
all individuals: 3388
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5234
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5855
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4428
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2086
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variant carriers: 0

GenotypeDepth
all individuals: 5905
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2677
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1167
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4457
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1527
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3570
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 117
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1905
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2999
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1449
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1362
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 844
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 164
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 575
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variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 582
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1096
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46275
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1211
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 675
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1010
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506931886678722e-5
allele num: 66360
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15824
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -1.126e0

DP
type: SiteQuality
SIO_000300: 3.500743e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.869e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.664e0

QD
type: SiteQuality
SIO_000300: 1.474e1

FS
type: SiteQuality
SIO_000300: 2.898e0

VQSLOD
type: SiteQuality
SIO_000300: -1.682e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.75e-1