11-83641510-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83641510
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83641510
    reference: chr 11
allele count: 1
allele frequency: 8.292699107705576e-6
allele num: 120588
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.1042T>A
  hgvsp: ENSP00000432894.1:p.Tyr348Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.304T>A
  hgvsp: ENSP00000443248.1:p.Tyr102Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.943T>A
  hgvsp: ENSP00000433848.1:p.Tyr315Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.859T>A
  hgvsp: ENSP00000381353.3:p.Tyr287Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1357T>A
  hgvsp: ENSP00000441994.1:p.Tyr453Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.872+32418T>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1159T>A
  hgvsp: ENSP00000280241.8:p.Tyr387Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1159T>A
  hgvsp: ENSP00000381346.2:p.Tyr387Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.1042T>A
  hgvsp: ENSP00000435849.1:p.Tyr348Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1357T>A
  hgvsp: ENSP00000365272.2:p.Tyr453Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-513T>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.1042T>A
  hgvsp: ENSP00000381355.2:p.Tyr348Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1320T>A
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10868
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4366
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8390
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11875
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr453Asn
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD

11-83641520-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83641520
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83641520
    reference: chr 11
allele count: 2
allele frequency: 1.660936435962596e-5
allele num: 120414
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-523G>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.872+32408G>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.294G>A
  hgvsp: ENST00000537455.1:c.294G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.1032G>A
  hgvsp: ENST00000524982.1:c.1032G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.1032G>A
  hgvsp: ENST00000398309.2:c.1032G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.933G>A
  hgvsp: ENST00000531015.1:c.933G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1310G>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.1032G>A
  hgvsp: ENST00000532653.1:c.1032G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1347G>A
  hgvsp: ENST00000376104.2:c.1347G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1149G>A
  hgvsp: ENST00000280241.8:c.1149G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1149G>A
  hgvsp: ENST00000398301.2:c.1149G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1347G>A
  hgvsp: ENST00000543673.1:c.1347G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.849G>A
  hgvsp: ENST00000330014.6:c.849G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2916
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6490
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1797
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8387
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4365
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11766
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro449Pro
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

11-83641521-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83641521
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83641521
    reference: chr 11
allele count: 101
allele frequency: 8.389679863107006e-4
allele num: 120386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1346C>T
  hgvsp: ENSP00000441994.1:p.Pro449Leu
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1148C>T
  hgvsp: ENSP00000381346.2:p.Pro383Leu
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.1031C>T
  hgvsp: ENSP00000432894.1:p.Pro344Leu
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1346C>T
  hgvsp: ENSP00000365272.2:p.Pro449Leu
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.1031C>T
  hgvsp: ENSP00000435849.1:p.Pro344Leu
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.872+32407C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1309C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.932C>T
  hgvsp: ENSP00000433848.1:p.Pro311Leu
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1148C>T
  hgvsp: ENSP00000280241.8:p.Pro383Leu
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.1031C>T
  hgvsp: ENSP00000381355.2:p.Pro344Leu
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.848C>T
  hgvsp: ENSP00000381353.3:p.Pro283Leu
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.293C>T
  hgvsp: ENSP00000443248.1:p.Pro98Leu
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-524C>T
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 10832
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6804
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4356
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6480
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro449Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: QD

11-83641522-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83641522
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83641522
    reference: chr 11
allele count: 4
allele frequency: 3.324136555529701e-5
allele num: 120332
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1345C>T
  hgvsp: ENSP00000441994.1:p.Pro449Ser
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.292C>T
  hgvsp: ENSP00000443248.1:p.Pro98Ser
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.1030C>T
  hgvsp: ENSP00000381355.2:p.Pro344Ser
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.847C>T
  hgvsp: ENSP00000381353.3:p.Pro283Ser
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1147C>T
  hgvsp: ENSP00000280241.8:p.Pro383Ser
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.1030C>T
  hgvsp: ENSP00000435849.1:p.Pro344Ser
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1147C>T
  hgvsp: ENSP00000381346.2:p.Pro383Ser
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1345C>T
  hgvsp: ENSP00000365272.2:p.Pro449Ser
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1308C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.1030C>T
  hgvsp: ENSP00000432894.1:p.Pro344Ser
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-525C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.872+32406C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.931C>T
  hgvsp: ENSP00000433848.1:p.Pro311Ser
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1863
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2915
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10832
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6722
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6491
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11723
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8378
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro449Ser
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

11-83641524-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83641524
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83641524
    reference: chr 11
allele count: 1
allele frequency: 8.311032063961702e-6
allele num: 120322
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1306C>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.1028C>A
  hgvsp: ENSP00000432894.1:p.Pro343His
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-527C>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1145C>A
  hgvsp: ENSP00000280241.8:p.Pro382His
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1343C>A
  hgvsp: ENSP00000365272.2:p.Pro448His
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1145C>A
  hgvsp: ENSP00000381346.2:p.Pro382His
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1343C>A
  hgvsp: ENSP00000441994.1:p.Pro448His
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.1028C>A
  hgvsp: ENSP00000435849.1:p.Pro343His
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.929C>A
  hgvsp: ENSP00000433848.1:p.Pro310His
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.872+32404C>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.1028C>A
  hgvsp: ENSP00000381355.2:p.Pro343His
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.845C>A
  hgvsp: ENSP00000381353.3:p.Pro282His
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.290C>A
  hgvsp: ENSP00000443248.1:p.Pro97His
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4364
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6722
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11734
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2915
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro448His
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP

11-83641530-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83641530
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83641530
    reference: chr 11
allele count: 1
allele frequency: 8.325008325008325e-6
allele num: 120120
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1304-4C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.872+32398C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.927-4C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1341-4C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.843-4C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-529-4C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.1026-4C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.1026-4C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1143-4C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.288-4C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1341-4C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.1026-4C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1143-4C>T
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6487
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1863
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6457
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2918
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10800
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8372
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4363
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1341-4C>T
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-83641530-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83641530
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83641530
    reference: chr 11
allele count: 2
allele frequency: 1.665001665001665e-5
allele num: 120120
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.1026-4C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1341-4C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1143-4C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.1026-4C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1304-4C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.1026-4C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.843-4C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1143-4C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.927-4C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.288-4C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1341-4C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.872+32398C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-529-4C>G
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2918
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6487
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8372
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6457
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10800
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1341-4C>G
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: VQSLOD

11-83641539-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83641539
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83641539
    reference: chr 11
allele count: 1
allele frequency: 8.343206127250579e-6
allele num: 119858
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.1026-13C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1304-13C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1143-13C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.1026-13C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.872+32389C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1341-13C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.1026-13C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.843-13C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.927-13C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1341-13C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.288-13C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-529-13C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1143-13C>G
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5966
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6485
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2918
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11296
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1863
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10702
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4359
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

11-83641542-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83641542
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83641542
    reference: chr 11
allele count: 2
allele frequency: 1.669867245553978e-5
allele num: 119770
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1143-16C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.288-16C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1143-16C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1341-16C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1304-16C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.843-16C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.1026-16C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.1026-16C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.872+32386C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.1026-16C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1341-16C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.927-16C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-529-16C>T
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6480
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11123
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4358
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8366
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2917
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5795
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10657
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ

11-83641542-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83641542
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83641542
    reference: chr 11
allele count: 3
allele frequency: 2.504800868330968e-5
allele num: 119770
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1143-16C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.1026-16C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1341-16C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.927-16C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1341-16C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.872+32386C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1304-16C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-529-16C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.288-16C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.843-16C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1143-16C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.1026-16C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.1026-16C>G
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10657
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4358
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11123
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6480
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5795
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8366
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum

11-83641545-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83641545
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83641545
    reference: chr 11
allele count: 1
allele frequency: 8.353102342209896e-6
allele num: 119716
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1341-19C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.1026-19C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1341-19C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1143-19C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.288-19C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.872+32383C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1304-19C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.1026-19C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.1026-19C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.843-19C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.927-19C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1143-19C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-529-19C>T
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11005
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10623
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6479
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2916
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1648
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4360
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8365
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: African
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

11-83641553-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83641553
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83641553
    reference: chr 11
allele count: 1
allele frequency: 8.373386029842748e-6
allele num: 119426
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1341-27A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-529-27A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1341-27A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.872+32375A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.843-27A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.1026-27A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.1026-27A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1143-27A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1304-27A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.1026-27A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.288-27A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1143-27A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.927-27A>G
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8354
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4358
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1863
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4793
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10507
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2321
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

11-83641555-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83641555
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83641555
    reference: chr 11
allele count: 1
allele frequency: 8.3760511944249e-6
allele num: 119388
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.1026-29A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1143-29A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1341-29A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1341-29A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-529-29A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1304-29A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.872+32373A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.1026-29A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.288-29A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.1026-29A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.843-29A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.927-29A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1143-29A>G
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8350
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10485
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4800
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10456
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4359
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6481
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

11-83641560-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83641560
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83641560
    reference: chr 11
allele count: 1
allele frequency: 8.387572971884856e-6
allele num: 119224
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1143-34C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1341-34C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.927-34C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.843-34C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.1026-34C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.872+32368C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.288-34C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-529-34C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1341-34C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1304-34C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1143-34C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.1026-34C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.1026-34C>T
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8346
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10071
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2521
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4410
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4358
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10350
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2086
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6475
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2919
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD

11-83641570-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83641570
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83641570
    reference: chr 11
allele count: 2
allele frequency: 1.68401199016537e-5
allele num: 118764
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.872+32358A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.288-44A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1143-44A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.1026-44A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1341-44A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.1026-44A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.927-44A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1143-44A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1341-44A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.1026-44A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.843-44A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1304-44A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-529-44A>G
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9808
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2526
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4346
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4710
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6458
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8274
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2919
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD

11-83641574-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83641574
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83641574
    reference: chr 11
allele count: 14
allele frequency: 1.180697286082952e-4
allele num: 118574
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.1026-48T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1304-48T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.288-48T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1341-48T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1143-48T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.1026-48T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.1026-48T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.872+32354T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.927-48T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.843-48T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1341-48T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1143-48T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-529-48T>C
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2530
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5372
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4342
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6457
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1793
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2917
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8537
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3269
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8243
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

11-83641575-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83641575
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83641575
    reference: chr 11
allele count: 15
allele frequency: 1.265587823357689e-4
allele num: 118522
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.1026-49C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.1026-49C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.927-49C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.872+32353C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1143-49C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.843-49C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1341-49C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-529-49C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.288-49C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1304-49C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.1026-49C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1143-49C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1341-49C>T
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8463
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9515
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5513
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4341
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6454
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2526
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8240
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP

11-83641578-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83641578
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83641578
    reference: chr 11
allele count: 6
allele frequency: 5.072365751386447e-5
allele num: 118288
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.288-52T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.872+32350T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1304-52T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-529-52T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.1026-52T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1341-52T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.843-52T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.1026-52T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1341-52T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1143-52T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1143-52T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.927-52T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.1026-52T>C
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8499
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5636
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3247
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2917
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1863
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2519
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6455
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8215
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4339
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

11-83673879-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83673879
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83673879
    reference: chr 11
allele count: 1
allele frequency: 8.303992559622666e-6
allele num: 120424
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1142+49A>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-530+49A>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.287+49A>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1142+49A>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1340+49A>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.842+49A>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.926+49A>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.1025+49A>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.1025+49A>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1303+49A>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.872+49A>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1340+49A>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.1025+49A>T
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5611
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5445
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4981
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3036
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2738
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3841
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4858
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2323
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3988
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5682
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5182
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3009
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD

11-83673894-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83673894
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83673894
    reference: chr 11
allele count: 3
allele frequency: 2.489833181176861e-5
allele num: 120490
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1340+34C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.287+34C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1303+34C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1142+34C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.926+34C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.1025+34C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.872+34C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.1025+34C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.842+34C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.1025+34C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-530+34C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1142+34C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1340+34C>G
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3190
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4860
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3284
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5682
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3988
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5611
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5444
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3009
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/11-83673897-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83673897
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83673897
    reference: chr 11
allele count: 2
allele frequency: 1.66013679527193e-5
allele num: 120472
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.1025+31G>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.926+31G>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.842+31G>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1142+31G>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.872+31G>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.1025+31G>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-530+31G>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1142+31G>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.1025+31G>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1303+31G>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.287+31G>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1340+31G>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1340+31G>T
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3054
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3847
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3008
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4859
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5180
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5444
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3214
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4982
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3341
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5683
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5611
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3989
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum

11-83673904-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83673904
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83673904
    reference: chr 11
allele count: 1
allele frequency: 8.294349888855711e-6
allele num: 120564
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1340+24T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1142+24T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1340+24T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.872+24T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.1025+24T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-530+24T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1142+24T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1303+24T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.1025+24T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.287+24T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.1025+24T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.842+24T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.926+24T>C
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2914
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5610
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5444
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4983
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3284
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3467
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3056
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3008
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5683
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: VQSLOD

11-83673905-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83673905
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83673905
    reference: chr 11
allele count: 18
allele frequency: 1.492908683752177e-4
allele num: 120570
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.842+23T>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1340+23T>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1142+23T>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.872+23T>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.1025+23T>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1340+23T>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.1025+23T>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.287+23T>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1303+23T>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-530+23T>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1142+23T>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.926+23T>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.1025+23T>A
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2923
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3989
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4983
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3469
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3007
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3846
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5609
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5444
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3276
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5187
  bin: 9.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 5685
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

11-83673907-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83673907
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83673907
    reference: chr 11
allele count: 1
allele frequency: 8.293799555452344e-6
allele num: 120572
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-530+21A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.287+21A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1340+21A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1142+21A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1303+21A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.872+21A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.842+21A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.1025+21A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.926+21A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1340+21A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.1025+21A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1142+21A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.1025+21A>G
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5177
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3844
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4861
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2928
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3297
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5611
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5447
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3057
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5688
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3991
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

11-83673919-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83673919
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83673919
    reference: chr 11
allele count: 1
allele frequency: 8.290636555074699e-6
allele num: 120618
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.1025+9T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.1025+9T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.872+9T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1340+9T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.842+9T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1142+9T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1303+9T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1142+9T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.926+9T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.1025+9T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.287+9T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1340+9T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-530+9T>C
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2957
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3068
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3259
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3588
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5610
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5688
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3991
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3008
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4987
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4861
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3846
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum

11-83673931-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83673931
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83673931
    reference: chr 11
allele count: 101
allele frequency: 8.370073258859018e-4
allele num: 120668
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1337C>T
  hgvsp: ENSP00000441994.1:p.Thr446Ile
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1139C>T
  hgvsp: ENSP00000280241.8:p.Thr380Ile
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1300C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.1022C>T
  hgvsp: ENSP00000435849.1:p.Thr341Ile
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.1022C>T
  hgvsp: ENSP00000381355.2:p.Thr341Ile
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-533C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1337C>T
  hgvsp: ENSP00000365272.2:p.Thr446Ile
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.1022C>T
  hgvsp: ENSP00000432894.1:p.Thr341Ile
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.869C>T
  hgvsp: ENSP00000402275.2:p.Thr290Ile
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.839C>T
  hgvsp: ENSP00000381353.3:p.Thr280Ile
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.923C>T
  hgvsp: ENSP00000433848.1:p.Thr308Ile
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1139C>T
  hgvsp: ENSP00000381346.2:p.Thr380Ile
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.284C>T
  hgvsp: ENSP00000443248.1:p.Thr95Ile
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2978
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3067
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3988
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5683
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5238
  bin: 9.75e1
  variant carriers: 88
genotype depth: GenotypeDepth
  all individuals: 3289
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3845
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4980
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr446Ile
num of homozygotes: 1
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
reference allele: G
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

11-83673934-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83673934
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83673934
    reference: chr 11
allele count: 1
allele frequency: 8.286926544683108e-6
allele num: 120672
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1334A>G
  hgvsp: ENSP00000365272.2:p.Tyr445Cys
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1136A>G
  hgvsp: ENSP00000381346.2:p.Tyr379Cys
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.1019A>G
  hgvsp: ENSP00000432894.1:p.Tyr340Cys
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-536A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.836A>G
  hgvsp: ENSP00000381353.3:p.Tyr279Cys
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.866A>G
  hgvsp: ENSP00000402275.2:p.Tyr289Cys
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.1019A>G
  hgvsp: ENSP00000381355.2:p.Tyr340Cys
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.920A>G
  hgvsp: ENSP00000433848.1:p.Tyr307Cys
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1334A>G
  hgvsp: ENSP00000441994.1:p.Tyr445Cys
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.1019A>G
  hgvsp: ENSP00000435849.1:p.Tyr340Cys
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1136A>G
  hgvsp: ENSP00000280241.8:p.Tyr379Cys
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.281A>G
  hgvsp: ENSP00000443248.1:p.Tyr94Cys
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1297A>G
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5159
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3846
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2984
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3003
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5455
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4988
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3614
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3293
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5693
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr445Cys
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

11-83673938-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83673938
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83673938
    reference: chr 11
allele count: 7
allele frequency: 5.800656302827405e-5
allele num: 120676
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.1015G>A
  hgvsp: ENSP00000381355.2:p.Asp339Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1293G>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.832G>A
  hgvsp: ENSP00000381353.3:p.Asp278Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.1015G>A
  hgvsp: ENSP00000432894.1:p.Asp339Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.277G>A
  hgvsp: ENSP00000443248.1:p.Asp93Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-540G>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.916G>A
  hgvsp: ENSP00000433848.1:p.Asp306Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1132G>A
  hgvsp: ENSP00000381346.2:p.Asp378Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1132G>A
  hgvsp: ENSP00000280241.8:p.Asp378Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.862G>A
  hgvsp: ENSP00000402275.2:p.Asp288Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1330G>A
  hgvsp: ENSP00000441994.1:p.Asp444Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.1015G>A
  hgvsp: ENSP00000435849.1:p.Asp339Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1330G>A
  hgvsp: ENSP00000365272.2:p.Asp444Asn
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5161
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3624
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5695
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3293
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3844
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2983
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3079
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5616
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4987
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp444Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

11-83673939-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83673939
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83673939
    reference: chr 11
allele count: 2
allele frequency: 1.657330372236402e-5
allele num: 120676
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1131C>T
  hgvsp: ENST00000280241.8:c.1131C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-541C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.1014C>T
  hgvsp: ENST00000398309.2:c.1014C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.1014C>T
  hgvsp: ENST00000524982.1:c.1014C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.831C>T
  hgvsp: ENST00000330014.6:c.831C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1329C>T
  hgvsp: ENST00000543673.1:c.1329C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.861C>T
  hgvsp: ENST00000418306.2:c.861C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1131C>T
  hgvsp: ENST00000398301.2:c.1131C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1292C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1329C>T
  hgvsp: ENST00000376104.2:c.1329C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.915C>T
  hgvsp: ENST00000531015.1:c.915C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.1014C>T
  hgvsp: ENST00000532653.1:c.1014C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.276C>T
  hgvsp: ENST00000537455.1:c.276C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5617
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2989
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5456
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3621
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5695
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3843
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4862
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5158
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp443Asp
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/11-83673941-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83673941
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83673941
    reference: chr 11
allele count: 1
allele frequency: 8.287613333112331e-6
allele num: 120662
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1327G>T
  hgvsp: ENSP00000365272.2:p.Asp443Tyr
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1327G>T
  hgvsp: ENSP00000441994.1:p.Asp443Tyr
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.1012G>T
  hgvsp: ENSP00000381355.2:p.Asp338Tyr
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1129G>T
  hgvsp: ENSP00000280241.8:p.Asp377Tyr
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.913G>T
  hgvsp: ENSP00000433848.1:p.Asp305Tyr
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.829G>T
  hgvsp: ENSP00000381353.3:p.Asp277Tyr
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.1012G>T
  hgvsp: ENSP00000435849.1:p.Asp338Tyr
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-543G>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1129G>T
  hgvsp: ENSP00000381346.2:p.Asp377Tyr
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.859G>T
  hgvsp: ENSP00000402275.2:p.Asp287Tyr
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.1012G>T
  hgvsp: ENSP00000432894.1:p.Asp338Tyr
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1290G>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.274G>T
  hgvsp: ENSP00000443248.1:p.Asp92Tyr
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5159
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4862
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3993
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5456
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4987
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2989
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5695
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3296
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3005
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp443Tyr
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

11-83673941-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83673941
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83673941
    reference: chr 11
allele count: 3
allele frequency: 2.486283999933699e-5
allele num: 120662
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.913G>A
  hgvsp: ENSP00000433848.1:p.Asp305Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.859G>A
  hgvsp: ENSP00000402275.2:p.Asp287Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.1012G>A
  hgvsp: ENSP00000432894.1:p.Asp338Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1327G>A
  hgvsp: ENSP00000365272.2:p.Asp443Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.274G>A
  hgvsp: ENSP00000443248.1:p.Asp92Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1327G>A
  hgvsp: ENSP00000441994.1:p.Asp443Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1129G>A
  hgvsp: ENSP00000280241.8:p.Asp377Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.829G>A
  hgvsp: ENSP00000381353.3:p.Asp277Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-543G>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.1012G>A
  hgvsp: ENSP00000381355.2:p.Asp338Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1290G>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.1012G>A
  hgvsp: ENSP00000435849.1:p.Asp338Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1129G>A
  hgvsp: ENSP00000381346.2:p.Asp377Asn
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5617
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5159
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5456
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3844
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2989
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3082
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3621
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4987
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5695
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp443Asn
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

11-83673942-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83673942
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83673942
    reference: chr 11
allele count: 3
allele frequency: 2.485871961021528e-5
allele num: 120682
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.858C>T
  hgvsp: ENST00000418306.2:c.858C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.1011C>T
  hgvsp: ENST00000398309.2:c.1011C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.1011C>T
  hgvsp: ENST00000532653.1:c.1011C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1289C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.273C>T
  hgvsp: ENST00000537455.1:c.273C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.912C>T
  hgvsp: ENST00000531015.1:c.912C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.1011C>T
  hgvsp: ENST00000524982.1:c.1011C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1128C>T
  hgvsp: ENST00000398301.2:c.1128C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1326C>T
  hgvsp: ENST00000543673.1:c.1326C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-544C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1128C>T
  hgvsp: ENST00000280241.8:c.1128C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1326C>T
  hgvsp: ENST00000376104.2:c.1326C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.828C>T
  hgvsp: ENST00000330014.6:c.828C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3621
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2991
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3299
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3082
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4862
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5617
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5158
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3845
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5456
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp442Asp
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ

http://identifiers.org/exac.variant/11-83673947-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83673947
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83673947
    reference: chr 11
allele count: 1
allele frequency: 8.285965232089886e-6
allele num: 120686
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.1006G>T
  hgvsp: ENSP00000432894.1:p.Val336Phe
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.1006G>T
  hgvsp: ENSP00000435849.1:p.Val336Phe
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1321G>T
  hgvsp: ENSP00000365272.2:p.Val441Phe
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.1006G>T
  hgvsp: ENSP00000381355.2:p.Val336Phe
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1123G>T
  hgvsp: ENSP00000381346.2:p.Val375Phe
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1123G>T
  hgvsp: ENSP00000280241.8:p.Val375Phe
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-549G>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1321G>T
  hgvsp: ENSP00000441994.1:p.Val441Phe
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.853G>T
  hgvsp: ENSP00000402275.2:p.Val285Phe
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.823G>T
  hgvsp: ENSP00000381353.3:p.Val275Phe
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1284G>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.907G>T
  hgvsp: ENSP00000433848.1:p.Val303Phe
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.268G>T
  hgvsp: ENSP00000443248.1:p.Val90Phe
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4987
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4862
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3005
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5456
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3849
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5618
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3299
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5696
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2997
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3993
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val441Phe
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

11-83673952-A-ATGT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83673952
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83673955
    reference: chr 11
allele count: 1
allele frequency: 8.285141427364165e-6
allele num: 120698
alternate allele: ATGT
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.998_1000dupACA
  hgvsp: ENSP00000381355.2:p.His333_Met334insAsn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-557_-555dupACA
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.998_1000dupACA
  hgvsp: ENSP00000432894.1:p.His333_Met334insAsn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.815_817dupACA
  hgvsp: ENSP00000381353.3:p.His272_Met273insAsn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1115_1117dupACA
  hgvsp: ENSP00000280241.8:p.His372_Met373insAsn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.899_901dupACA
  hgvsp: ENSP00000433848.1:p.His300_Met301insAsn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: inframe_insertion
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1313_1315dupACA
  hgvsp: ENSP00000365272.2:p.His438_Met439insAsn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1313_1315dupACA
  hgvsp: ENSP00000441994.1:p.His438_Met439insAsn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.260_262dupACA
  hgvsp: ENSP00000443248.1:p.His87_Met88insAsn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.845_847dupACA
  hgvsp: ENSP00000402275.2:p.His282_Met283insAsn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1115_1117dupACA
  hgvsp: ENSP00000381346.2:p.His372_Met373insAsn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1276_1278dupACA
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.998_1000dupACA
  hgvsp: ENSP00000435849.1:p.His333_Met334insAsn
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: inframe insertion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3004
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4988
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3086
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5616
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5457
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5696
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4863
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3301
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3847
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His438_Met439insAsn
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/11-83673952-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83673952
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83673952
    reference: chr 11
allele count: 1
allele frequency: 8.285141427364165e-6
allele num: 120698
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.1001T>G
  hgvsp: ENSP00000435849.1:p.Met334Arg
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.1001T>G
  hgvsp: ENSP00000432894.1:p.Met334Arg
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.818T>G
  hgvsp: ENSP00000381353.3:p.Met273Arg
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.848T>G
  hgvsp: ENSP00000402275.2:p.Met283Arg
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1118T>G
  hgvsp: ENSP00000381346.2:p.Met373Arg
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.263T>G
  hgvsp: ENSP00000443248.1:p.Met88Arg
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1316T>G
  hgvsp: ENSP00000365272.2:p.Met439Arg
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.1001T>G
  hgvsp: ENSP00000381355.2:p.Met334Arg
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1279T>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1118T>G
  hgvsp: ENSP00000280241.8:p.Met373Arg
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-554T>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.902T>G
  hgvsp: ENSP00000433848.1:p.Met301Arg
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1316T>G
  hgvsp: ENSP00000441994.1:p.Met439Arg
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3847
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5616
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4863
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3301
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2994
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3994
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5457
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5696
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met439Arg
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

11-83673952-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83673952
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83673952
    reference: chr 11
allele count: 1
allele frequency: 8.285141427364165e-6
allele num: 120698
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1316T>A
  hgvsp: ENSP00000441994.1:p.Met439Lys
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.263T>A
  hgvsp: ENSP00000443248.1:p.Met88Lys
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1118T>A
  hgvsp: ENSP00000280241.8:p.Met373Lys
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.902T>A
  hgvsp: ENSP00000433848.1:p.Met301Lys
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1316T>A
  hgvsp: ENSP00000365272.2:p.Met439Lys
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-554T>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.1001T>A
  hgvsp: ENSP00000435849.1:p.Met334Lys
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.818T>A
  hgvsp: ENSP00000381353.3:p.Met273Lys
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1279T>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.848T>A
  hgvsp: ENSP00000402275.2:p.Met283Lys
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1118T>A
  hgvsp: ENSP00000381346.2:p.Met373Lys
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.1001T>A
  hgvsp: ENSP00000432894.1:p.Met334Lys
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.1001T>A
  hgvsp: ENSP00000381355.2:p.Met334Lys
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4988
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3847
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4863
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3994
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2994
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3301
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5457
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met439Lys
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

11-83673954-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83673954
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83673954
    reference: chr 11
allele count: 451
allele frequency: 3.736474954847475e-3
allele num: 120702
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.816C>T
  hgvsp: ENST00000330014.6:c.816C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1116C>T
  hgvsp: ENST00000280241.8:c.1116C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-556C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.999C>T
  hgvsp: ENST00000524982.1:c.999C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1314C>T
  hgvsp: ENST00000543673.1:c.1314C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1314C>T
  hgvsp: ENST00000376104.2:c.1314C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1277C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.999C>T
  hgvsp: ENST00000398309.2:c.999C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.846C>T
  hgvsp: ENST00000418306.2:c.846C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.261C>T
  hgvsp: ENST00000537455.1:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.999C>T
  hgvsp: ENST00000532653.1:c.999C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1116C>T
  hgvsp: ENST00000398301.2:c.1116C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.900C>T
  hgvsp: ENST00000531015.1:c.900C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3841
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4960
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 9.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3611
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3084
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3977
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5443
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5594
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.His438His
num of homozygotes: 5
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP

11-83673968-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83673968
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83673968
    reference: chr 11
allele count: 8
allele frequency: 6.628003314001656e-5
allele num: 120700
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-570C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1300C>G
  hgvsp: ENSP00000365272.2:p.Pro434Ala
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.802C>G
  hgvsp: ENSP00000381353.3:p.Pro268Ala
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.985C>G
  hgvsp: ENSP00000435849.1:p.Pro329Ala
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1300C>G
  hgvsp: ENSP00000441994.1:p.Pro434Ala
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1263C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.985C>G
  hgvsp: ENSP00000432894.1:p.Pro329Ala
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.247C>G
  hgvsp: ENSP00000443248.1:p.Pro83Ala
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.832C>G
  hgvsp: ENSP00000402275.2:p.Pro278Ala
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.985C>G
  hgvsp: ENSP00000381355.2:p.Pro329Ala
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1102C>G
  hgvsp: ENSP00000280241.8:p.Pro368Ala
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.886C>G
  hgvsp: ENSP00000433848.1:p.Pro296Ala
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1102C>G
  hgvsp: ENSP00000381346.2:p.Pro368Ala
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5632
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4988
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3124
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3870
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5472
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5721
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2999
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro434Ala
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/11-83673975-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83673975
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83673975
    reference: chr 11
allele count: 4
allele frequency: 3.314550878355983e-5
allele num: 120680
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1095G>T
  hgvsp: ENSP00000381346.2:p.Arg365Ser
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1095G>T
  hgvsp: ENSP00000280241.8:p.Arg365Ser
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.978G>T
  hgvsp: ENSP00000435849.1:p.Arg326Ser
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-577G>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.978G>T
  hgvsp: ENSP00000432894.1:p.Arg326Ser
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1293G>T
  hgvsp: ENSP00000441994.1:p.Arg431Ser
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.240G>T
  hgvsp: ENSP00000443248.1:p.Arg80Ser
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.825G>T
  hgvsp: ENSP00000402275.2:p.Arg275Ser
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.879G>T
  hgvsp: ENSP00000433848.1:p.Arg293Ser
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.978G>T
  hgvsp: ENSP00000381355.2:p.Arg326Ser
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.795G>T
  hgvsp: ENSP00000381353.3:p.Arg265Ser
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1256G>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1293G>T
  hgvsp: ENSP00000365272.2:p.Arg431Ser
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3129
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2999
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5473
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5721
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3271
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4893
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5631
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg431Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum

11-83673981-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83673981
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83673981
    reference: chr 11
allele count: 1
allele frequency: 8.285553309249991e-6
allele num: 120692
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1089A>T
  hgvsp: ENST00000280241.8:c.1089A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.972A>T
  hgvsp: ENST00000398309.2:c.972A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.819A>T
  hgvsp: ENST00000418306.2:c.819A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1089A>T
  hgvsp: ENST00000398301.2:c.1089A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.234A>T
  hgvsp: ENST00000537455.1:c.234A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.972A>T
  hgvsp: ENST00000524982.1:c.972A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1250A>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1287A>T
  hgvsp: ENST00000376104.2:c.1287A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-583A>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.789A>T
  hgvsp: ENST00000330014.6:c.789A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.873A>T
  hgvsp: ENST00000531015.1:c.873A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1287A>T
  hgvsp: ENST00000543673.1:c.1287A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.972A>T
  hgvsp: ENST00000532653.1:c.972A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3259
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4003
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3033
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5721
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5631
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2999
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4988
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5030
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3876
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3640
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3120
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro429Pro
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

11-83673981-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83673981
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83673981
    reference: chr 11
allele count: 1
allele frequency: 8.285553309249991e-6
allele num: 120692
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1287A>C
  hgvsp: ENST00000376104.2:c.1287A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1250A>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.234A>C
  hgvsp: ENST00000537455.1:c.234A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1089A>C
  hgvsp: ENST00000280241.8:c.1089A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.819A>C
  hgvsp: ENST00000418306.2:c.819A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-583A>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1287A>C
  hgvsp: ENST00000543673.1:c.1287A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.972A>C
  hgvsp: ENST00000524982.1:c.972A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.789A>C
  hgvsp: ENST00000330014.6:c.789A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1089A>C
  hgvsp: ENST00000398301.2:c.1089A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.972A>C
  hgvsp: ENST00000398309.2:c.972A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.972A>C
  hgvsp: ENST00000532653.1:c.972A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.873A>C
  hgvsp: ENST00000531015.1:c.873A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4895
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3640
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5631
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2999
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2144
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3033
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5030
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4003
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4988
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3259
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro429Pro
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

11-83673993-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83673993
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83673993
    reference: chr 11
allele count: 2
allele frequency: 1.657000828500414e-5
allele num: 120700
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1077A>G
  hgvsp: ENST00000398301.2:c.1077A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1238A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.777A>G
  hgvsp: ENST00000330014.6:c.777A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1275A>G
  hgvsp: ENST00000376104.2:c.1275A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.807A>G
  hgvsp: ENST00000418306.2:c.807A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.960A>G
  hgvsp: ENST00000398309.2:c.960A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-595A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.960A>G
  hgvsp: ENST00000532653.1:c.960A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1275A>G
  hgvsp: ENST00000543673.1:c.1275A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.960A>G
  hgvsp: ENST00000524982.1:c.960A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1077A>G
  hgvsp: ENST00000280241.8:c.1077A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.222A>G
  hgvsp: ENST00000537455.1:c.222A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.861A>G
  hgvsp: ENST00000531015.1:c.861A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3873
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2999
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4893
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3032
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4003
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3263
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5721
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3119
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3643
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5473
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro425Pro
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD

11-83674011-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83674011
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83674011
    reference: chr 11
allele count: 4
allele frequency: 3.314221323699997e-5
allele num: 120692
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.843A>G
  hgvsp: ENST00000531015.1:c.843A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1220A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.942A>G
  hgvsp: ENST00000532653.1:c.942A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1257A>G
  hgvsp: ENST00000543673.1:c.1257A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1059A>G
  hgvsp: ENST00000280241.8:c.1059A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-613A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.942A>G
  hgvsp: ENST00000398309.2:c.942A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.789A>G
  hgvsp: ENST00000418306.2:c.789A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1257A>G
  hgvsp: ENST00000376104.2:c.1257A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381344
  ensembl transcript: ENST00000398299
  gene symbol: DLG2
  hgvsc: ENST00000398299.1:c.693A>G
  hgvsp: ENST00000398299.1:c.693A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.759A>G
  hgvsp: ENST00000330014.6:c.759A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.942A>G
  hgvsp: ENST00000524982.1:c.942A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1059A>G
  hgvsp: ENST00000398301.2:c.1059A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.204A>G
  hgvsp: ENST00000537455.1:c.204A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3107
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5476
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4988
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5719
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3035
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3000
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4004
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3643
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu419Glu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

11-83674018-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83674018
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83674018
    reference: chr 11
allele count: 1
allele frequency: 8.286102548805144e-6
allele num: 120684
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.935C>A
  hgvsp: ENSP00000432894.1:p.Thr312Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1213C>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.197C>A
  hgvsp: ENSP00000443248.1:p.Thr66Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.752C>A
  hgvsp: ENSP00000381353.3:p.Thr251Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.782C>A
  hgvsp: ENSP00000402275.2:p.Thr261Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1250C>A
  hgvsp: ENSP00000365272.2:p.Thr417Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.935C>A
  hgvsp: ENSP00000381355.2:p.Thr312Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1052C>A
  hgvsp: ENSP00000280241.8:p.Thr351Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.935C>A
  hgvsp: ENSP00000435849.1:p.Thr312Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1052C>A
  hgvsp: ENSP00000381346.2:p.Thr351Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1250C>A
  hgvsp: ENSP00000441994.1:p.Thr417Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-620C>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381344
  ensembl transcript: ENST00000398299
  gene symbol: DLG2
  hgvsc: ENST00000398299.1:c.686C>A
  hgvsp: ENSP00000381344.1:p.Thr229Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.836C>A
  hgvsp: ENSP00000433848.1:p.Thr279Asn
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3112
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2999
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5478
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4003
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5632
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2143
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5031
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr417Asn
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

11-83674021-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83674021
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83674021
    reference: chr 11
allele count: 3
allele frequency: 2.486242789895909e-5
allele num: 120664
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1049G>A
  hgvsp: ENSP00000381346.2:p.Gly350Asp
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.749G>A
  hgvsp: ENSP00000381353.3:p.Gly250Asp
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1049G>A
  hgvsp: ENSP00000280241.8:p.Gly350Asp
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1210G>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1247G>A
  hgvsp: ENSP00000365272.2:p.Gly416Asp
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.932G>A
  hgvsp: ENSP00000381355.2:p.Gly311Asp
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.932G>A
  hgvsp: ENSP00000432894.1:p.Gly311Asp
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.779G>A
  hgvsp: ENSP00000402275.2:p.Gly260Asp
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.932G>A
  hgvsp: ENSP00000435849.1:p.Gly311Asp
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1247G>A
  hgvsp: ENSP00000441994.1:p.Gly416Asp
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.833G>A
  hgvsp: ENSP00000433848.1:p.Gly278Asp
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-623G>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381344
  ensembl transcript: ENST00000398299
  gene symbol: DLG2
  hgvsc: ENST00000398299.1:c.683G>A
  hgvsp: ENSP00000381344.1:p.Gly228Asp
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.194G>A
  hgvsp: ENSP00000443248.1:p.Gly65Asp
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2143
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3655
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5033
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5718
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4893
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3107
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly416Asp
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

11-83674026-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83674026
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83674026
    reference: chr 11
allele count: 1
allele frequency: 8.285004142502071e-6
allele num: 120700
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.927C>T
  hgvsp: ENST00000398309.2:c.927C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-628C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381344
  ensembl transcript: ENST00000398299
  gene symbol: DLG2
  hgvsc: ENST00000398299.1:c.678C>T
  hgvsp: ENST00000398299.1:c.678C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1044C>T
  hgvsp: ENST00000280241.8:c.1044C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1242C>T
  hgvsp: ENST00000376104.2:c.1242C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.744C>T
  hgvsp: ENST00000330014.6:c.744C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1205C>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.189C>T
  hgvsp: ENST00000537455.1:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.927C>T
  hgvsp: ENST00000524982.1:c.927C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.927C>T
  hgvsp: ENST00000532653.1:c.927C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1044C>T
  hgvsp: ENST00000398301.2:c.1044C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1242C>T
  hgvsp: ENST00000543673.1:c.1242C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.774C>T
  hgvsp: ENST00000418306.2:c.774C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.828C>T
  hgvsp: ENST00000531015.1:c.828C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3875
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4003
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5719
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2998
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3107
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4988
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3657
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn414Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD

11-83674029-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83674029
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83674029
    reference: chr 11
allele count: 1
allele frequency: 8.285141427364165e-6
allele num: 120698
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.825C>A
  hgvsp: ENST00000531015.1:c.825C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.924C>A
  hgvsp: ENST00000532653.1:c.924C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.924C>A
  hgvsp: ENST00000398309.2:c.924C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1239C>A
  hgvsp: ENST00000543673.1:c.1239C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1041C>A
  hgvsp: ENST00000280241.8:c.1041C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.924C>A
  hgvsp: ENST00000524982.1:c.924C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1041C>A
  hgvsp: ENST00000398301.2:c.1041C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.741C>A
  hgvsp: ENST00000330014.6:c.741C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1239C>A
  hgvsp: ENST00000376104.2:c.1239C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1202C>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.771C>A
  hgvsp: ENST00000418306.2:c.771C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.186C>A
  hgvsp: ENST00000537455.1:c.186C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-631C>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381344
  ensembl transcript: ENST00000398299
  gene symbol: DLG2
  hgvsc: ENST00000398299.1:c.675C>A
  hgvsp: ENST00000398299.1:c.675C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3656
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5476
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2143
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3253
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4892
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4988
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly413Gly
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS

11-83674038-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83674038
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83674038
    reference: chr 11
allele count: 4
allele frequency: 3.314441019522058e-5
allele num: 120684
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.816A>G
  hgvsp: ENST00000531015.1:c.816A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.915A>G
  hgvsp: ENST00000532653.1:c.915A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1032A>G
  hgvsp: ENST00000280241.8:c.1032A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1230A>G
  hgvsp: ENST00000543673.1:c.1230A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.732A>G
  hgvsp: ENST00000330014.6:c.732A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-640A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.915A>G
  hgvsp: ENST00000398309.2:c.915A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.762A>G
  hgvsp: ENST00000418306.2:c.762A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1032A>G
  hgvsp: ENST00000398301.2:c.1032A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1230A>G
  hgvsp: ENST00000376104.2:c.1230A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.915A>G
  hgvsp: ENST00000524982.1:c.915A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.177A>G
  hgvsp: ENST00000537455.1:c.177A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381344
  ensembl transcript: ENST00000398299
  gene symbol: DLG2
  hgvsc: ENST00000398299.1:c.666A>G
  hgvsp: ENST00000398299.1:c.666A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1193A>G
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5718
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3648
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4987
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3019
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2143
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4892
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3108
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5635
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu410Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

11-83674040-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83674040
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83674040
    reference: chr 11
allele count: 3
allele frequency: 2.485830764641543e-5
allele num: 120684
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.913C>G
  hgvsp: ENSP00000432894.1:p.Leu305Val
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.913C>G
  hgvsp: ENSP00000381355.2:p.Leu305Val
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1228C>G
  hgvsp: ENSP00000365272.2:p.Leu410Val
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.814C>G
  hgvsp: ENSP00000433848.1:p.Leu272Val
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.913C>G
  hgvsp: ENSP00000435849.1:p.Leu305Val
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.760C>G
  hgvsp: ENSP00000402275.2:p.Leu254Val
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.175C>G
  hgvsp: ENSP00000443248.1:p.Leu59Val
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1030C>G
  hgvsp: ENSP00000381346.2:p.Leu344Val
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1228C>G
  hgvsp: ENSP00000441994.1:p.Leu410Val
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381344
  ensembl transcript: ENST00000398299
  gene symbol: DLG2
  hgvsc: ENST00000398299.1:c.664C>G
  hgvsp: ENSP00000381344.1:p.Leu222Val
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-642C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1030C>G
  hgvsp: ENSP00000280241.8:p.Leu344Val
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1191C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.730C>G
  hgvsp: ENSP00000381353.3:p.Leu244Val
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5031
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5635
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3107
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3021
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3256
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5476
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4988
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu410Val
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/11-83674041-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83674041
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83674041
    reference: chr 11
allele count: 1
allele frequency: 8.285965232089886e-6
allele num: 120686
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.912T>G
  hgvsp: ENSP00000432894.1:p.His304Gln
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1190T>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.912T>G
  hgvsp: ENSP00000435849.1:p.His304Gln
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1029T>G
  hgvsp: ENSP00000381346.2:p.His343Gln
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.813T>G
  hgvsp: ENSP00000433848.1:p.His271Gln
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.912T>G
  hgvsp: ENSP00000381355.2:p.His304Gln
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1227T>G
  hgvsp: ENSP00000365272.2:p.His409Gln
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1227T>G
  hgvsp: ENSP00000441994.1:p.His409Gln
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.174T>G
  hgvsp: ENSP00000443248.1:p.His58Gln
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.729T>G
  hgvsp: ENSP00000381353.3:p.His243Gln
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.759T>G
  hgvsp: ENSP00000402275.2:p.His253Gln
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-643T>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1029T>G
  hgvsp: ENSP00000280241.8:p.His343Gln
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381344
  ensembl transcript: ENST00000398299
  gene symbol: DLG2
  hgvsc: ENST00000398299.1:c.663T>G
  hgvsp: ENSP00000381344.1:p.His221Gln
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4988
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3256
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5029
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3877
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2998
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3638
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5635
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His409Gln
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff

11-83674042-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83674042
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83674042
    reference: chr 11
allele count: 1
allele frequency: 8.286239870071759e-6
allele num: 120682
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1226A>G
  hgvsp: ENSP00000365272.2:p.His409Arg
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1028A>G
  hgvsp: ENSP00000280241.8:p.His343Arg
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.173A>G
  hgvsp: ENSP00000443248.1:p.His58Arg
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1226A>G
  hgvsp: ENSP00000441994.1:p.His409Arg
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.911A>G
  hgvsp: ENSP00000435849.1:p.His304Arg
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.812A>G
  hgvsp: ENSP00000433848.1:p.His271Arg
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381344
  ensembl transcript: ENST00000398299
  gene symbol: DLG2
  hgvsc: ENST00000398299.1:c.662A>G
  hgvsp: ENSP00000381344.1:p.His221Arg
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-644A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.911A>G
  hgvsp: ENSP00000381355.2:p.His304Arg
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.758A>G
  hgvsp: ENSP00000402275.2:p.His253Arg
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.911A>G
  hgvsp: ENSP00000432894.1:p.His304Arg
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.728A>G
  hgvsp: ENSP00000381353.3:p.His243Arg
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1189A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1028A>G
  hgvsp: ENSP00000381346.2:p.His343Arg
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5635
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4895
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3109
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3875
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3024
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3637
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5028
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.His409Arg
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

11-83674043-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83674043
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83674043
    reference: chr 11
allele count: 1
allele frequency: 8.287201246395068e-6
allele num: 120668
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.757C>A
  hgvsp: ENSP00000402275.2:p.His253Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1225C>A
  hgvsp: ENSP00000365272.2:p.His409Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.910C>A
  hgvsp: ENSP00000432894.1:p.His304Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.910C>A
  hgvsp: ENSP00000435849.1:p.His304Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1027C>A
  hgvsp: ENSP00000381346.2:p.His343Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.811C>A
  hgvsp: ENSP00000433848.1:p.His271Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.172C>A
  hgvsp: ENSP00000443248.1:p.His58Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.910C>A
  hgvsp: ENSP00000381355.2:p.His304Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1225C>A
  hgvsp: ENSP00000441994.1:p.His409Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1027C>A
  hgvsp: ENSP00000280241.8:p.His343Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.727C>A
  hgvsp: ENSP00000381353.3:p.His243Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1188C>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381344
  ensembl transcript: ENST00000398299
  gene symbol: DLG2
  hgvsc: ENST00000398299.1:c.661C>A
  hgvsp: ENSP00000381344.1:p.His221Asn
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-645C>A
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5635
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5476
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3875
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4894
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3110
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4988
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5717
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His409Asn
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: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum

11-83674048-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83674048
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83674048
    reference: chr 11
allele count: 1
allele frequency: 8.286926544683108e-6
allele num: 120672
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.806A>G
  hgvsp: ENSP00000433848.1:p.Glu269Gly
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1220A>G
  hgvsp: ENSP00000441994.1:p.Glu407Gly
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.905A>G
  hgvsp: ENSP00000381355.2:p.Glu302Gly
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1220A>G
  hgvsp: ENSP00000365272.2:p.Glu407Gly
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381344
  ensembl transcript: ENST00000398299
  gene symbol: DLG2
  hgvsc: ENST00000398299.1:c.656A>G
  hgvsp: ENSP00000381344.1:p.Glu219Gly
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1022A>G
  hgvsp: ENSP00000280241.8:p.Glu341Gly
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.905A>G
  hgvsp: ENSP00000432894.1:p.Glu302Gly
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.905A>G
  hgvsp: ENSP00000435849.1:p.Glu302Gly
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.722A>G
  hgvsp: ENSP00000381353.3:p.Glu241Gly
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.752A>G
  hgvsp: ENSP00000402275.2:p.Glu251Gly
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1022A>G
  hgvsp: ENSP00000381346.2:p.Glu341Gly
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1183A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.167A>G
  hgvsp: ENSP00000443248.1:p.Glu56Gly
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-650A>G
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3876
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4002
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3632
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5717
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2143
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5476
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2999
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5635
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3252
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu407Gly
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

11-83674052-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83674052
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83674052
    reference: chr 11
allele count: 1
allele frequency: 8.288712431410904e-6
allele num: 120646
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.802A>G
  hgvsp: ENSP00000433848.1:p.Met268Val
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1216A>G
  hgvsp: ENSP00000365272.2:p.Met406Val
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.901A>G
  hgvsp: ENSP00000432894.1:p.Met301Val
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.718A>G
  hgvsp: ENSP00000381353.3:p.Met240Val
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1179A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.901A>G
  hgvsp: ENSP00000435849.1:p.Met301Val
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381344
  ensembl transcript: ENST00000398299
  gene symbol: DLG2
  hgvsc: ENST00000398299.1:c.652A>G
  hgvsp: ENSP00000381344.1:p.Met218Val
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.163A>G
  hgvsp: ENSP00000443248.1:p.Met55Val
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.901A>G
  hgvsp: ENSP00000381355.2:p.Met301Val
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.748A>G
  hgvsp: ENSP00000402275.2:p.Met250Val
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1216A>G
  hgvsp: ENSP00000441994.1:p.Met406Val
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1018A>G
  hgvsp: ENSP00000381346.2:p.Met340Val
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1018A>G
  hgvsp: ENSP00000280241.8:p.Met340Val
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-654A>G
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4987
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3106
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3241
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5635
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3634
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3028
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3876
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2999
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met406Val
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum

11-83674053-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83674053
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83674053
    reference: chr 11
allele count: 1
allele frequency: 8.287475966319697e-6
allele num: 120664
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.900A>C
  hgvsp: ENST00000524982.1:c.900A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.162A>C
  hgvsp: ENST00000537455.1:c.162A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1017A>C
  hgvsp: ENST00000280241.8:c.1017A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1178A>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381344
  ensembl transcript: ENST00000398299
  gene symbol: DLG2
  hgvsc: ENST00000398299.1:c.651A>C
  hgvsp: ENST00000398299.1:c.651A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1215A>C
  hgvsp: ENST00000543673.1:c.1215A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-655A>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.900A>C
  hgvsp: ENST00000532653.1:c.900A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.801A>C
  hgvsp: ENST00000531015.1:c.801A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.717A>C
  hgvsp: ENST00000330014.6:c.717A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.900A>C
  hgvsp: ENST00000398309.2:c.900A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.747A>C
  hgvsp: ENST00000418306.2:c.747A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1215A>C
  hgvsp: ENST00000376104.2:c.1215A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1017A>C
  hgvsp: ENST00000398301.2:c.1017A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5475
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2999
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3106
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5635
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5718
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2144
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3635
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro405Pro
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

11-83674073-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83674073
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83674073
    reference: chr 11
allele count: 1
allele frequency: 8.292699107705576e-6
allele num: 120588
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.887-7C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1165-7C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.788-7C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1004-7C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381344
  ensembl transcript: ENST00000398299
  gene symbol: DLG2
  hgvsc: ENST00000398299.1:c.638-7C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.704-7C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1202-7C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.887-7C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1004-7C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1202-7C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-668-7C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.887-7C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.734-7C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.149-7C>G
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2999
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3100
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5027
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3595
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4002
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3144
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1202-7C>G
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

11-83674078-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83674078
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83674078
    reference: chr 11
allele count: 1
allele frequency: 8.29531314807134e-6
allele num: 120550
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.887-12C>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381344
  ensembl transcript: ENST00000398299
  gene symbol: DLG2
  hgvsc: ENST00000398299.1:c.638-12C>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1004-12C>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1202-12C>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.887-12C>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1165-12C>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.734-12C>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-668-12C>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.704-12C>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.788-12C>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.149-12C>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1202-12C>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1004-12C>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.887-12C>A
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5716
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3871
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2999
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4988
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4892
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3095
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5476
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3565
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5026
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4002
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP

11-83674081-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83674081
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83674081
    reference: chr 11
allele count: 1
allele frequency: 8.295726041943191e-6
allele num: 120544
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1004-15T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.887-15T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1004-15T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.734-15T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.704-15T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.887-15T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.887-15T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.788-15T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1202-15T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381344
  ensembl transcript: ENST00000398299
  gene symbol: DLG2
  hgvsc: ENST00000398299.1:c.638-15T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1202-15T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.149-15T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1165-15T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-668-15T>C
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5476
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5026
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2957
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3870
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3531
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2999
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3094
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3068
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4891
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5717
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: African
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

11-83674088-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83674088
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83674088
    reference: chr 11
allele count: 1
allele frequency: 8.297928836962294e-6
allele num: 120512
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.887-22C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.887-22C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.887-22C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1202-22C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.704-22C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1202-22C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1004-22C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1165-22C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.734-22C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.149-22C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.788-22C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-668-22C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1004-22C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381344
  ensembl transcript: ENST00000398299
  gene symbol: DLG2
  hgvsc: ENST00000398299.1:c.638-22C>G
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5026
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3491
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3001
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2989
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3091
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5716
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2925
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5636
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4894
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3869
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

11-83674094-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83674094
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83674094
    reference: chr 11
allele count: 1
allele frequency: 8.300132802124834e-6
allele num: 120480
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.887-28T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.734-28T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.887-28T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381344
  ensembl transcript: ENST00000398299
  gene symbol: DLG2
  hgvsc: ENST00000398299.1:c.638-28T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.704-28T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.149-28T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1202-28T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1004-28T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1165-28T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-668-28T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.788-28T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.887-28T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1202-28T>C
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1004-28T>C
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3082
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5637
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5477
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2999
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3328
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2815
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4986
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3868
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2875
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ

http://identifiers.org/exac.variant/11-83674097-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83674097
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83674097
    reference: chr 11
allele count: 2
allele frequency: 1.660633033312299e-5
allele num: 120436
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1004-31G>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.887-31G>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.887-31G>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.887-31G>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1165-31G>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1004-31G>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.734-31G>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1202-31G>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-668-31G>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381344
  ensembl transcript: ENST00000398299
  gene symbol: DLG2
  hgvsc: ENST00000398299.1:c.638-31G>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.149-31G>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.788-31G>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.704-31G>T
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1202-31G>T
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3244
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3085
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5636
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2855
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4987
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5714
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2686
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3873
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4001
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD

11-83674099-T-TTATTGTA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83674099
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83674106
    reference: chr 11
allele count: 2
allele frequency: 1.660853678790898e-5
allele num: 120420
alternate allele: TTATTGTA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1165-34_1165-33insTACAATA
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.887-34_887-33insTACAATA
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1202-34_1202-33insTACAATA
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381344
  ensembl transcript: ENST00000398299
  gene symbol: DLG2
  hgvsc: ENST00000398299.1:c.638-34_638-33insTACAATA
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1004-34_1004-33insTACAATA
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.887-34_887-33insTACAATA
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.734-34_734-33insTACAATA
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.788-34_788-33insTACAATA
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1004-34_1004-33insTACAATA
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.887-34_887-33insTACAATA
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.704-34_704-33insTACAATA
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.149-34_149-33insTACAATA
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-668-34_-668-33insTACAATA
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1202-34_1202-33insTACAATA
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5637
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3183
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4892
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4983
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2622
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3868
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3000
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5478
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3077
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD

11-83674103-A-AGTTAATTGGATT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83674103
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83674115
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 120392
alternate allele: AGTTAATTGGATT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381344
  ensembl transcript: ENST00000398299
  gene symbol: DLG2
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4983
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3073
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2994
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2453
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5715
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4000
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2750
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4888
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5027
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2999
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3866
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5639
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5479
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

11-83674104-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83674104
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83674104
    reference: chr 11
allele count: 2
allele frequency: 1.664115023630433e-5
allele num: 120184
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.887-38A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.704-38A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.887-38A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1165-38A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.788-38A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-668-38A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1202-38A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.149-38A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.734-38A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381344
  ensembl transcript: ENST00000398299
  gene symbol: DLG2
  hgvsc: ENST00000398299.1:c.638-38A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.887-38A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1004-38A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1202-38A>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1004-38A>G
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5476
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5636
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4887
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3875
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4984
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5028
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2958
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2748
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5717
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3077
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum

11-83674107-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83674107
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83674107
    reference: chr 11
allele count: 13
allele frequency: 1.081890812250333e-4
allele num: 120160
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1202-41C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381344
  ensembl transcript: ENST00000398299
  gene symbol: DLG2
  hgvsc: ENST00000398299.1:c.638-41C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1165-41C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-668-41C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1004-41C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.149-41C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.734-41C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.887-41C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.887-41C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1004-41C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.788-41C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.887-41C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.704-41C>G
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1202-41C>G
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3873
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5632
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3067
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2856
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5027
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4885
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2703
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3000
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5476
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum

11-83674107-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 83674107
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 83674107
    reference: chr 11
allele count: 1
allele frequency: 8.322237017310253e-6
allele num: 120160
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000432894
  ensembl transcript: ENST00000524982
  gene symbol: DLG2
  hgvsc: ENST00000524982.1:c.887-41C>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000402275
  ensembl transcript: ENST00000418306
  gene symbol: DLG2
  hgvsc: ENST00000418306.2:c.734-41C>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381355
  ensembl transcript: ENST00000398309
  gene symbol: DLG2
  hgvsc: ENST00000398309.2:c.887-41C>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl transcript: ENST00000529111
  gene symbol: DLG2
  hgvsc: ENST00000529111.1:n.1165-41C>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000435849
  ensembl transcript: ENST00000532653
  gene symbol: DLG2
  hgvsc: ENST00000532653.1:c.887-41C>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000441994
  ensembl transcript: ENST00000543673
  gene symbol: DLG2
  hgvsc: ENST00000543673.1:c.1202-41C>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000280241
  ensembl transcript: ENST00000280241
  gene symbol: DLG2
  hgvsc: ENST00000280241.8:c.1004-41C>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365272
  ensembl transcript: ENST00000376104
  gene symbol: DLG2
  hgvsc: ENST00000376104.2:c.1202-41C>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381353
  ensembl transcript: ENST00000330014
  gene symbol: DLG2
  hgvsc: ENST00000330014.6:c.704-41C>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000433848
  ensembl transcript: ENST00000531015
  gene symbol: DLG2
  hgvsc: ENST00000531015.1:c.788-41C>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000443248
  ensembl transcript: ENST00000537455
  gene symbol: DLG2
  hgvsc: ENST00000537455.1:c.149-41C>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000365274
  ensembl transcript: ENST00000376106
  gene symbol: DLG2
  hgvsc: ENST00000376106.3:c.-668-41C>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381346
  ensembl transcript: ENST00000398301
  gene symbol: DLG2
  hgvsc: ENST00000398301.2:c.1004-41C>A
  variant of: http://identifiers.org/hgnc/2901
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150672
  ensembl protein: ENSP00000381344
  ensembl transcript: ENST00000398299
  gene symbol: DLG2
  hgvsc: ENST00000398299.1:c.638-41C>A
  variant of: http://identifiers.org/hgnc/2901
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5027
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2856
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4885
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3873
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5476
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4000
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5632
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3067
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5715
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4984
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
reference allele: G

GenotypeDepth
all individuals: 120
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7040
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6489
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2916
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 328
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1796
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 30
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22484
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4328
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14962
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2259
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2885
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5602
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4073
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3468
bin: 9.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16446
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5008254539997e-5
allele num: 66630
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.972e1

DP
type: SiteQuality
SIO_000300: 2.433202e6

FS
type: SiteQuality
SIO_000300: 1.072e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.11e0

MQRankSum
type: SiteQuality
SIO_000300: -2.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.25e-1

QD
type: SiteQuality
SIO_000300: 1.497e1

VQSLOD
type: SiteQuality
SIO_000300: 1.97e0

GenotypeDepth
all individuals: 328
bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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African
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Latino
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Other
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European (Non-Finnish)
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FS
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InbreedingCoeff
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DP
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QD
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MQRankSum
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MQ
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele num: 6614
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Other
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Latino
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South Asian
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African
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European (Non-Finnish)
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East Asian
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InbreedingCoeff
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MQRankSum
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VQSLOD
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FS
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ReadPosRankSum
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BaseQRankSum
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MQ
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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East Asian
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South Asian
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Other
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European (Finnish)
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MQ
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ClippingRankSum
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FS
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DP
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MQRankSum
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QD
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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European (Non-Finnish)
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African
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Latino
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Other
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VQSLOD
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MQRankSum
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FS
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BaseQRankSum
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QD
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ReadPosRankSum
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ClippingRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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European (Finnish)
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Other
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QD
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BaseQRankSum
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MQRankSum
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FS
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VQSLOD
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InbreedingCoeff
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DP
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MQ
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ReadPosRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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South Asian
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European (Finnish)
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Latino
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East Asian
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MQ
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MQRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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QD
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DP
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15994
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.021659174499387e-4
allele num: 9788
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66396
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.101e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e0

MQRankSum
type: SiteQuality
SIO_000300: 9.31e-1

InbreedingCoeff
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SIO_000300: 5.0e-4

QD
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SIO_000300: 1.787e1

MQ
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SIO_000300: 5.957e1

BaseQRankSum
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SIO_000300: -2.7e-1

ClippingRankSum
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SIO_000300: 7.4e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.543e-1

DP
type: SiteQuality
SIO_000300: 2.409445e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9788
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66382
num of homozygotes: 0

South Asian
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allele frequency: 1.255965837729214e-4
allele num: 15924
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

MQRankSum
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SIO_000300: 5.1e-1

InbreedingCoeff
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DP
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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FS
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SIO_000300: 9.879e0

QD
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BaseQRankSum
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SIO_000300: 2.0e-2

MQ
type: SiteQuality
SIO_000300: 5.929e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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variant carriers: 3

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

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

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

East Asian
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allele count: 3
allele frequency: 3.484320557491289e-4
allele num: 8610
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66382
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 2.87e-1

InbreedingCoeff
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ReadPosRankSum
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MQ
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MQRankSum
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VQSLOD
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DP
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FS
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SIO_000300: 9.879e0

QD
type: SiteQuality
SIO_000300: 1.46e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.0e-2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 70
bin: 4.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506704836522525e-5
allele num: 66370
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15894
num of homozygotes: 0

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

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

Other
type: Population
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

VQSLOD
type: SiteQuality
SIO_000300: 5.21e-1

BaseQRankSum
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MQ
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SIO_000300: 5.935e1

DP
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SIO_000300: 2.401071e6

FS
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SIO_000300: 1.146e0

ReadPosRankSum
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SIO_000300: 7.4e-1

MQRankSum
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SIO_000300: 9.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

QD
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SIO_000300: 9.369999999999999e0

GenotypeDepth
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15720
num of homozygotes: 0

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

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.508887346470713e-5
allele num: 66274
num of homozygotes: 0

VQSLOD
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DP
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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FS
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MQRankSum
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InbreedingCoeff
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QD
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MQ
type: SiteQuality
SIO_000300: 5.903e1

GenotypeDepth
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variant carriers: 0

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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bin: 6.25e1
variant carriers: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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Other
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
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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
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.50879628232596e-5
allele num: 66278
num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

Other
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East Asian
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South Asian
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European (Non-Finnish)
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allele frequency: 0.0e0
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African
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allele num: 9780
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European (Finnish)
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num of homozygotes: 0

ClippingRankSum
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MQ
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InbreedingCoeff
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MQRankSum
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VQSLOD
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DP
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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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variant carriers: 0

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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bin: 8.75e1
variant carriers: 0

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

Latino
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allele count: 1
allele frequency: 8.670019074041963e-5
allele num: 11534
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.02291325695581e-4
allele num: 9776
num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15270
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66106
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.78e0

FS
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SIO_000300: 5.542e0

InbreedingCoeff
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SIO_000300: 2.2e-3

VQSLOD
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SIO_000300: 5.1e-2

ClippingRankSum
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SIO_000300: -2.48e-1

ReadPosRankSum
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SIO_000300: 9.85e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.88e-1

DP
type: SiteQuality
SIO_000300: 2.352348e6

QD
type: SiteQuality
SIO_000300: 1.728e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 13

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 14
allele frequency: 2.120505286116749e-4
allele num: 66022
num of homozygotes: 0

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

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

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
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SIO_000300: 3.19e0

DP
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SIO_000300: 2.346467e6

ReadPosRankSum
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FS
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SIO_000300: 0.0e0

MQRankSum
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InbreedingCoeff
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SIO_000300: 1.5e-3

QD
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ClippingRankSum
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SIO_000300: -5.590000000000001e-1

BaseQRankSum
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SIO_000300: 6.8e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 15

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1579
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15140
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 1.817575959528642e-4
allele num: 66022
num of homozygotes: 0

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

Latino
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allele count: 3
allele frequency: 2.601908065915004e-4
allele num: 11530
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

MQ
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SIO_000300: 6.0e1

QD
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SIO_000300: 1.418e1

ReadPosRankSum
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SIO_000300: 4.61e-1

BaseQRankSum
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ClippingRankSum
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SIO_000300: 7.7e-2

VQSLOD
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MQRankSum
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SIO_000300: 5.570000000000001e-1

FS
type: SiteQuality
SIO_000300: 1.654e0

DP
type: SiteQuality
SIO_000300: 2.345384e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 850
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 5.206525511975009e-4
allele num: 11524
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9750
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65942
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15020
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

DP
type: SiteQuality
SIO_000300: 2.343686e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.04e-1

BaseQRankSum
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SIO_000300: 4.79e0

VQSLOD
type: SiteQuality
SIO_000300: 3.75e-1

FS
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SIO_000300: 1.252e0

QD
type: SiteQuality
SIO_000300: 1.614e1

InbreedingCoeff
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SIO_000300: 1.0e-3

MQRankSum
type: SiteQuality
SIO_000300: -4.75e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16404
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66564
num of homozygotes: 0

African
type: Population
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allele frequency: 1.02082482645978e-4
allele num: 9796
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 900
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

MQRankSum
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SIO_000300: -1.226e0

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

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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variant carriers: 3

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.667013347200555e-5
allele num: 11538
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: 1
allele frequency: 1.501636784094663e-5
allele num: 66594
num of homozygotes: 0

South Asian
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num of homozygotes: 0

Other
type: Population
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allele frequency: 1.111111111111111e-3
allele num: 900
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East Asian
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InbreedingCoeff
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MQ
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ReadPosRankSum
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MQRankSum
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FS
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QD
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VQSLOD
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DP
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ClippingRankSum
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BaseQRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.003634397621121e-5
allele num: 66586
num of homozygotes: 0

Other
type: Population
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ReadPosRankSum
type: SiteQuality
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MQRankSum
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VQSLOD
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MQ
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DP
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InbreedingCoeff
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BaseQRankSum
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FS
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QD
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ClippingRankSum
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SIO_000300: 9.72e-1

GenotypeDepth
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66612
num of homozygotes: 0

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

East Asian
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allele frequency: 1.160631383472609e-4
allele num: 8616
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -9.320000000000001e-1

InbreedingCoeff
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SIO_000300: 1.15e-2

ReadPosRankSum
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QD
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SIO_000300: 1.153e1

FS
type: SiteQuality
SIO_000300: 8.99e-1

BaseQRankSum
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SIO_000300: -3.726e0

MQ
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SIO_000300: 5.979e1

DP
type: SiteQuality
SIO_000300: 3.655516e6

MQRankSum
type: SiteQuality
SIO_000300: 7.38e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.78e-1

GenotypeDepth
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variant carriers: 0

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
all individuals: 998
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 17
allele frequency: 1.735402204981625e-3
allele num: 9796
num of homozygotes: 0

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

Latino
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allele count: 1
allele frequency: 8.655011251514626e-5
allele num: 11554
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66616
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.97e1

ReadPosRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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DP
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SIO_000300: 3.656319e6

FS
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SIO_000300: 0.0e0

QD
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SIO_000300: 1.408e1

BaseQRankSum
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SIO_000300: -1.925e0

ClippingRankSum
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SIO_000300: -5.570000000000001e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 40
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variant carriers: 0

GenotypeQuality
all individuals: 997
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66618
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.067961165048543e-5
allele num: 16480
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.51e-1

DP
type: SiteQuality
SIO_000300: 3.65599e6

QD
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SIO_000300: 1.3e1

FS
type: SiteQuality
SIO_000300: 3.914e0

VQSLOD
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SIO_000300: 5.7e-1

BaseQRankSum
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SIO_000300: 4.82e0

MQ
type: SiteQuality
SIO_000300: 5.986e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.299999999999999e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 2.29e-1

GenotypeDepth
all individuals: 5176
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 30
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variant carriers: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
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: 1
allele frequency: 1.500555205426008e-5
allele num: 66642
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.635e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.94e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.88e-1

InbreedingCoeff
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SIO_000300: 1.3e-3

MQRankSum
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SIO_000300: 1.69e0

BaseQRankSum
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SIO_000300: -9.287000000000001e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

QD
type: SiteQuality
SIO_000300: 1.455e1

DP
type: SiteQuality
SIO_000300: 3.658122e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.35e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 3

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 2
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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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 100

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 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: 16504
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.512401693889897e-4
allele num: 6612
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.111111111111111e-3
allele num: 900
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 94
allele frequency: 1.409887209023278e-3
allele num: 66672
num of homozygotes: 0

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

Latino
type: Population
allele count: 5
allele frequency: 4.323763403666552e-4
allele num: 11564
num of homozygotes: 1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.666573e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.79e-1

BaseQRankSum
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QD
type: SiteQuality
SIO_000300: 1.262e1

InbreedingCoeff
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SIO_000300: 8.3e-3

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.959e1

MQRankSum
type: SiteQuality
SIO_000300: 2.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.18e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1000
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8
bin: 3.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

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

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66676
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.966e1

BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 1.936e0

MQRankSum
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InbreedingCoeff
type: SiteQuality
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QD
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ReadPosRankSum
type: SiteQuality
SIO_000300: 6.21e-1

DP
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VQSLOD
type: SiteQuality
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ClippingRankSum
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GenotypeDepth
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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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variant carriers: 7

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2
bin: 1.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.049790041991602e-4
allele num: 66680
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

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

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

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
SIO_000300: 2.43e0

QD
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ClippingRankSum
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MQRankSum
type: SiteQuality
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InbreedingCoeff
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DP
type: SiteQuality
SIO_000300: 3.657795e6

BaseQRankSum
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SIO_000300: -5.0e-1

FS
type: SiteQuality
SIO_000300: 5.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.66e-1

MQ
type: SiteQuality
SIO_000300: 5.975e1

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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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

Latino
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allele count: 1
allele frequency: 8.64902266043937e-5
allele num: 11562
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499700059988002e-5
allele num: 66680
num of homozygotes: 0

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

DP
type: SiteQuality
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InbreedingCoeff
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MQRankSum
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VQSLOD
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BaseQRankSum
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FS
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ReadPosRankSum
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ClippingRankSum
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SIO_000300: -1.65e-1

MQ
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SIO_000300: 5.979e1

QD
type: SiteQuality
SIO_000300: 1.211e1

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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499745043342632e-5
allele num: 66678
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.93e-1

InbreedingCoeff
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SIO_000300: 4.5e-3

QD
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SIO_000300: 1.168e1

FS
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ClippingRankSum
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BaseQRankSum
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SIO_000300: -1.631e0

DP
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SIO_000300: 3.657561e6

MQ
type: SiteQuality
SIO_000300: 5.95e1

ReadPosRankSum
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SIO_000300: 1.15e0

VQSLOD
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SIO_000300: 3.09e0

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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.999490086685263e-5
allele num: 66678
num of homozygotes: 0

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.95e1

VQSLOD
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SIO_000300: 3.09e0

FS
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SIO_000300: 0.0e0

ClippingRankSum
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MQRankSum
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QD
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ReadPosRankSum
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InbreedingCoeff
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SIO_000300: 4.5e-3

DP
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SIO_000300: 3.657561e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.631e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

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

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

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

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

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

European (Finnish)
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allele count: 1
allele frequency: 1.512401693889897e-4
allele num: 6612
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66690
num of homozygotes: 0

East Asian
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allele count: 2
allele frequency: 2.320185614849188e-4
allele num: 8620
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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QD
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DP
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FS
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MQRankSum
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InbreedingCoeff
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SIO_000300: 1.0e-4

MQ
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SIO_000300: 5.972e1

GenotypeDepth
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bin: 9.75e1
variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499250374812594e-5
allele num: 66700
num of homozygotes: 0

African
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Other
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South Asian
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QD
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MQ
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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FS
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InbreedingCoeff
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SIO_000300: 3.7e-3

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9800
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: 8.653513326410523e-5
allele num: 11556
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 900
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66700
num of homozygotes: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 1.020408163265306e-4
allele num: 9800
num of homozygotes: 0

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

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66700
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.43e0

ClippingRankSum
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BaseQRankSum
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SIO_000300: 2.4e0

MQRankSum
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SIO_000300: -5.05e-1

DP
type: SiteQuality
SIO_000300: 3.657745e6

FS
type: SiteQuality
SIO_000300: 1.751e0

InbreedingCoeff
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SIO_000300: 3.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.9e-2

MQ
type: SiteQuality
SIO_000300: 5.838e1

QD
type: SiteQuality
SIO_000300: 1.24e1

GenotypeDepth
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bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 2.75e1
variant carriers: 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: 1.499250374812594e-5
allele num: 66700
num of homozygotes: 0

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

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.24e1

MQRankSum
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SIO_000300: -5.05e-1

MQ
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SIO_000300: 5.838e1

BaseQRankSum
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InbreedingCoeff
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SIO_000300: 3.5e-3

FS
type: SiteQuality
SIO_000300: 1.751e0

ReadPosRankSum
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SIO_000300: 7.9e-2

DP
type: SiteQuality
SIO_000300: 3.657745e6

VQSLOD
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SIO_000300: 3.43e0

ClippingRankSum
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SIO_000300: -1.452e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 414

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 446

GenotypeQuality
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GenotypeQuality
all individuals: 998
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variant carriers: 0

South Asian
type: Population
allele count: 25
allele frequency: 1.514233797698365e-3
allele num: 16510
num of homozygotes: 0

African
type: Population
allele count: 11
allele frequency: 1.122448979591837e-3
allele num: 9800
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 391
allele frequency: 5.861190226352871e-3
allele num: 66710
num of homozygotes: 4

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

Latino
type: Population
allele count: 10
allele frequency: 8.659508139937652e-4
allele num: 11548
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 11
allele frequency: 1.663138796492289e-3
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.333333333333334e-3
allele num: 900
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BaseQRankSum
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SIO_000300: -4.605e0

QD
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SIO_000300: 1.28e1

ReadPosRankSum
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VQSLOD
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MQRankSum
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SIO_000300: 3.44e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: 1.26e-2

MQ
type: SiteQuality
SIO_000300: 5.968e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.17e-1

DP
type: SiteQuality
SIO_000300: 3.694159e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 7

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 45093
bin: 9.75e1
variant carriers: 8

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

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.160092807424594e-4
allele num: 8620
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 4.239854633555421e-4
allele num: 16510
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.38e-1

MQ
type: SiteQuality
SIO_000300: 5.976e1

QD
type: SiteQuality
SIO_000300: 1.371e1

FS
type: SiteQuality
SIO_000300: 2.445e0

VQSLOD
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SIO_000300: 2.19e0

MQRankSum
type: SiteQuality
SIO_000300: 1.08e-1

BaseQRankSum
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SIO_000300: 2.34e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.8e-3

DP
type: SiteQuality
SIO_000300: 3.646468e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.0e-2

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 3

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1000
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variant carriers: 0

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

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

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

East Asian
type: Population
allele count: 4
allele frequency: 4.641448131817127e-4
allele num: 8618
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66708
num of homozygotes: 0

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

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

BaseQRankSum
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SIO_000300: -5.585e0

DP
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MQRankSum
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MQ
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InbreedingCoeff
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ClippingRankSum
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QD
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VQSLOD
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SIO_000300: 3.08e0

FS
type: SiteQuality
SIO_000300: 1.744e0

ReadPosRankSum
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SIO_000300: 7.98e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49902563333833e-5
allele num: 66710
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -3.46e-1

QD
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MQ
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BaseQRankSum
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DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 7.92e-1

VQSLOD
type: SiteQuality
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ReadPosRankSum
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SIO_000300: 5.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 4.34e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

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

South Asian
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allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 7.92e-1

DP
type: SiteQuality
SIO_000300: 3.645931e6

MQ
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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QD
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

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

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

Latino
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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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South Asian
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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QD
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ClippingRankSum
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FS
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MQ
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MQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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Latino
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European (Non-Finnish)
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East Asian
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Other
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FS
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MQ
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ReadPosRankSum
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VQSLOD
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MQRankSum
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DP
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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Other
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East Asian
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African
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European (Finnish)
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ReadPosRankSum
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InbreedingCoeff
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QD
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ClippingRankSum
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MQ
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VQSLOD
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BaseQRankSum
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FS
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MQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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East Asian
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South Asian
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African
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FS
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QD
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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MQ
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MQRankSum
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ReadPosRankSum
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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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European (Finnish)
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African
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East Asian
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European (Non-Finnish)
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Latino
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MQ
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InbreedingCoeff
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MQRankSum
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FS
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VQSLOD
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QD
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DP
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ReadPosRankSum
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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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European (Non-Finnish)
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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QD
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MQRankSum
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InbreedingCoeff
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SIO_000300: 2.0e-4

DP
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VQSLOD
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SIO_000300: 9.29e-1

FS
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SIO_000300: 0.0e0

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

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

East Asian
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allele count: 2
allele frequency: 2.328830926874709e-4
allele num: 8588
num of homozygotes: 0

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

Other
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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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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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VQSLOD
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SIO_000300: 8.51e-1

InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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MQ
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ReadPosRankSum
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SIO_000300: 9.9e-2

FS
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SIO_000300: 2.08e0

MQRankSum
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DP
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SIO_000300: 3.63091e6

QD
type: SiteQuality
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

African
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allele frequency: 1.022494887525562e-4
allele num: 9780
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502178158329578e-5
allele num: 66570
num of homozygotes: 0

South Asian
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QD
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SIO_000300: 4.9e-1

InbreedingCoeff
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MQRankSum
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BaseQRankSum
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MQ
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SIO_000300: 3.468e1

ReadPosRankSum
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DP
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SIO_000300: 3.629163e6

ClippingRankSum
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SIO_000300: 1.42e0

FS
type: SiteQuality
SIO_000300: 2.27e0

VQSLOD
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SIO_000300: -1.47e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66564
num of homozygotes: 0

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

African
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num of homozygotes: 0

Other
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South Asian
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MQRankSum
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InbreedingCoeff
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QD
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MQ
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BaseQRankSum
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FS
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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DP
type: SiteQuality
SIO_000300: 3.624972e6

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

Latino
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allele frequency: 3.497726477789437e-4
allele num: 11436
num of homozygotes: 0

South Asian
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European (Non-Finnish)
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allele frequency: 1.203550473897999e-4
allele num: 66470
num of homozygotes: 0

African
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Other
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East Asian
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European (Finnish)
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QD
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VQSLOD
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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DP
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MQ
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FS
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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