11-65426338-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65426338
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65426338
    reference: chr 11
allele count: 1
allele frequency: 8.29393713195654e-6
allele num: 120570
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.560-45A>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.744-45A>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.560-45A>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.593-45A>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.802-45A>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.*6-45A>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.*6-45A>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.*124-45A>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*258-45A>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.533-45A>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.560-45A>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.498-45A>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.467-45A>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431304
  ensembl transcript: ENST00000526257
  gene symbol: RELA
  hgvsc: ENST00000526257.1:c.78+799A>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.551-45A>C
  variant of: http://identifiers.org/hgnc/9955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7414
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12601
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3160
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4247
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13014
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1859
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum

11-65426338-T-TC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65426338
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65426339
    reference: chr 11
allele count: 1
allele frequency: 8.29393713195654e-6
allele num: 120570
alternate allele: TC
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.*6-46dupG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.560-46dupG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.498-46dupG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.*124-46dupG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.560-46dupG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.802-46dupG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.744-46dupG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*258-46dupG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.560-46dupG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.467-46dupG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.551-46dupG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.593-46dupG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.533-46dupG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431304
  ensembl transcript: ENST00000526257
  gene symbol: RELA
  hgvsc: ENST00000526257.1:c.78+798dupG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.*6-46dupG
  variant of: http://identifiers.org/hgnc/9955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7414
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3160
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8501
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4247
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP

11-65427087-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427087
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427087
    reference: chr 11
allele count: 3
allele frequency: 2.530236324072668e-5
allele num: 118566
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.497+50A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.*5+50A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.466+50A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.*5+50A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.559+50A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.801+50A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.*123+50A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.592+50A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*257+50A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.532+50A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.550+50A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.743+50A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.559+50A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.559+50A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431304
  ensembl transcript: ENST00000526257
  gene symbol: RELA
  hgvsc: ENST00000526257.1:c.78+50A>G
  variant of: http://identifiers.org/hgnc/9955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12113
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-65427099-CCA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427099
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427097
    reference: chr 11
allele count: 4
allele frequency: 3.370975897522333e-5
allele num: 118660
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.801+36_801+37delTG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.532+36_532+37delTG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.559+36_559+37delTG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.497+36_497+37delTG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.466+36_466+37delTG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.743+36_743+37delTG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.559+36_559+37delTG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431304
  ensembl transcript: ENST00000526257
  gene symbol: RELA
  hgvsc: ENST00000526257.1:c.78+36_78+37delTG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*257+36_*257+37delTG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.*5+36_*5+37delTG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.550+36_550+37delTG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.592+36_592+37delTG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.*123+36_*123+37delTG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.*5+36_*5+37delTG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.559+36_559+37delTG
  variant of: http://identifiers.org/hgnc/9955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2570
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12146
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30273
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
reference allele: CCA
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

11-65427106-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427106
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427106
    reference: chr 11
allele count: 4
allele frequency: 3.36802398033074e-5
allele num: 118764
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.559+31G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.550+31G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.532+31G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.743+31G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.497+31G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.801+31G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.466+31G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.559+31G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*257+31G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.*5+31G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.*5+31G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.*123+31G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.559+31G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.592+31G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431304
  ensembl transcript: ENST00000526257
  gene symbol: RELA
  hgvsc: ENST00000526257.1:c.78+31G>A
  variant of: http://identifiers.org/hgnc/9955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10686
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12151
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD

http://identifiers.org/exac.variant/11-65427115-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427115
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427115
    reference: chr 11
allele count: 2
allele frequency: 1.68219897049423e-5
allele num: 118892
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.550+22G>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.*5+22G>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.532+22G>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.*5+22G>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.743+22G>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.801+22G>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.592+22G>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.559+22G>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.*123+22G>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.559+22G>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.497+22G>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.559+22G>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.466+22G>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*257+22G>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431304
  ensembl transcript: ENST00000526257
  gene symbol: RELA
  hgvsc: ENST00000526257.1:c.78+22G>T
  variant of: http://identifiers.org/hgnc/9955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12166
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

11-65427118-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427118
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427118
    reference: chr 11
allele count: 4
allele frequency: 3.362531313572857e-5
allele num: 118958
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.466+19G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.532+19G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.497+19G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.*5+19G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.559+19G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.550+19G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431304
  ensembl transcript: ENST00000526257
  gene symbol: RELA
  hgvsc: ENST00000526257.1:c.78+19G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.*123+19G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.801+19G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*257+19G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.592+19G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.559+19G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.743+19G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.559+19G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.*5+19G>A
  variant of: http://identifiers.org/hgnc/9955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10972
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12170
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2560
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ReadPosRankSum

11-65427119-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427119
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427119
    reference: chr 11
allele count: 7
allele frequency: 5.876920493661322e-5
allele num: 119110
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.559+18C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.532+18C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.801+18C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.*5+18C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.743+18C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431304
  ensembl transcript: ENST00000526257
  gene symbol: RELA
  hgvsc: ENST00000526257.1:c.78+18C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.550+18C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.466+18C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.592+18C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.*123+18C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.559+18C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*257+18C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.559+18C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.497+18C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.*5+18C>T
  variant of: http://identifiers.org/hgnc/9955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11080
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2559
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12176
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30618
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD

11-65427121-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427121
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427121
    reference: chr 11
allele count: 1
allele frequency: 8.389120987902887e-6
allele num: 119202
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.559+16G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.559+16G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.532+16G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.550+16G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.592+16G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.559+16G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.*5+16G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.801+16G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*257+16G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.466+16G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.*123+16G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.*5+16G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431304
  ensembl transcript: ENST00000526257
  gene symbol: RELA
  hgvsc: ENST00000526257.1:c.78+16G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.743+16G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.497+16G>C
  variant of: http://identifiers.org/hgnc/9955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30649
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12173
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11165
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD

11-65427128-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427128
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427128
    reference: chr 11
allele count: 3
allele frequency: 2.513152162986295e-5
allele num: 119372
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.559+9C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.559+9C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.*5+9C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.801+9C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.532+9C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*257+9C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.559+9C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.*5+9C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.*123+9C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.550+9C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.497+9C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.466+9C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431304
  ensembl transcript: ENST00000526257
  gene symbol: RELA
  hgvsc: ENST00000526257.1:c.78+9C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.592+9C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.743+9C>T
  variant of: http://identifiers.org/hgnc/9955
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30701
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

11-65427168-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427168
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427168
    reference: chr 11
allele count: 2
allele frequency: 1.66591700401486e-5
allele num: 120054
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.466G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*226G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.436G>A
  hgvsp: ENSP00000437137.1:p.Ala146Thr
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.528G>A
  hgvsp: ENST00000526283.2:c.528G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.528G>A
  hgvsp: ENST00000525693.1:c.528G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.435G>A
  hgvsp: ENST00000527749.1:c.435G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.469G>A
  hgvsp: ENSP00000431153.1:p.Ala157Thr
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431304
  ensembl transcript: ENST00000526257
  gene symbol: RELA
  hgvsc: ENST00000526257.1:c.47G>A
  hgvsp: ENST00000526257.1:c.47G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.501G>A
  hgvsp: ENST00000534558.1:c.501G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.528G>A
  hgvsp: ENST00000406246.3:c.528G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.519G>A
  hgvsp: ENST00000308639.9:c.519G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.379G>A
  hgvsp: ENSP00000432922.1:p.Ala127Thr
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.770G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.561G>A
  hgvsp: ENST00000532999.1:c.561G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.712G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.*92G>A
  variant of: http://identifiers.org/hgnc/9955
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala157Thr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

11-65427169-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427169
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427169
    reference: chr 11
allele count: 3
allele frequency: 2.499583402766205e-5
allele num: 120020
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.468C>T
  hgvsp: ENST00000532879.1:c.468C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.500C>T
  hgvsp: ENSP00000434372.1:p.Pro167Leu
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.527C>T
  hgvsp: ENSP00000435290.1:p.Pro176Leu
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*225C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.527C>T
  hgvsp: ENSP00000384273.3:p.Pro176Leu
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.465C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431304
  ensembl transcript: ENST00000526257
  gene symbol: RELA
  hgvsc: ENST00000526257.1:c.46C>T
  hgvsp: ENSP00000431304.1:p.Pro16Leu
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.*91C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.527C>T
  hgvsp: ENSP00000432537.1:p.Pro176Leu
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.769C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.434C>T
  hgvsp: ENSP00000436545.1:p.Pro145Leu
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.711C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.518C>T
  hgvsp: ENSP00000311508.9:p.Pro173Leu
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.378C>T
  hgvsp: ENST00000527909.1:c.378C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.435C>T
  hgvsp: ENST00000529389.1:c.435C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.560C>T
  hgvsp: ENSP00000433526.1:p.Pro187Leu
  variant of: http://identifiers.org/hgnc/9955
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro176Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

11-65427177-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427177
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427177
    reference: chr 11
allele count: 1
allele frequency: 8.302613662781043e-6
allele num: 120444
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*217C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.519C>T
  hgvsp: ENST00000525693.1:c.519C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.519C>T
  hgvsp: ENST00000526283.2:c.519C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.*83C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.370C>T
  hgvsp: ENSP00000432922.1:p.Pro124Ser
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.492C>T
  hgvsp: ENST00000534558.1:c.492C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.426C>T
  hgvsp: ENST00000527749.1:c.426C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.460C>T
  hgvsp: ENSP00000431153.1:p.Pro154Ser
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.510C>T
  hgvsp: ENST00000308639.9:c.510C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.703C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.427C>T
  hgvsp: ENSP00000437137.1:p.Pro143Ser
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.519C>T
  hgvsp: ENST00000406246.3:c.519C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.457C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431304
  ensembl transcript: ENST00000526257
  gene symbol: RELA
  hgvsc: ENST00000526257.1:c.38C>T
  hgvsp: ENST00000526257.1:c.38C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.761C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.552C>T
  hgvsp: ENST00000532999.1:c.552C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro154Ser
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

11-65427177-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427177
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427177
    reference: chr 11
allele count: 1
allele frequency: 8.302613662781043e-6
allele num: 120444
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.457C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.370C>G
  hgvsp: ENSP00000432922.1:p.Pro124Ala
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.519C>G
  hgvsp: ENST00000525693.1:c.519C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.519C>G
  hgvsp: ENST00000406246.3:c.519C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.703C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.427C>G
  hgvsp: ENSP00000437137.1:p.Pro143Ala
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.519C>G
  hgvsp: ENST00000526283.2:c.519C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.552C>G
  hgvsp: ENST00000532999.1:c.552C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431304
  ensembl transcript: ENST00000526257
  gene symbol: RELA
  hgvsc: ENST00000526257.1:c.38C>G
  hgvsp: ENST00000526257.1:c.38C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.460C>G
  hgvsp: ENSP00000431153.1:p.Pro154Ala
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.*83C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.761C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.492C>G
  hgvsp: ENST00000534558.1:c.492C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.426C>G
  hgvsp: ENST00000527749.1:c.426C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*217C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.510C>G
  hgvsp: ENST00000308639.9:c.510C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12222
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro154Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/11-65427183-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427183
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427183
    reference: chr 11
allele count: 1
allele frequency: 8.294349888855711e-6
allele num: 120564
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.504G>T
  hgvsp: ENSP00000311508.9:p.Arg168Ser
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.513G>T
  hgvsp: ENSP00000384273.3:p.Arg171Ser
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*211G>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.513G>T
  hgvsp: ENSP00000435290.1:p.Arg171Ser
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431304
  ensembl transcript: ENST00000526257
  gene symbol: RELA
  hgvsc: ENST00000526257.1:c.32G>T
  hgvsp: ENSP00000431304.1:p.Arg11Ser
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.421G>T
  hgvsp: ENSP00000437137.1:p.Ala141Ser
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.546G>T
  hgvsp: ENSP00000433526.1:p.Arg182Ser
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.364G>T
  hgvsp: ENSP00000432922.1:p.Ala122Ser
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.486G>T
  hgvsp: ENSP00000434372.1:p.Arg162Ser
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.454G>T
  hgvsp: ENSP00000431153.1:p.Ala152Ser
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.755G>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.451G>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.*77G>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.420G>T
  hgvsp: ENSP00000436545.1:p.Arg140Ser
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.697G>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.513G>T
  hgvsp: ENSP00000432537.1:p.Arg171Ser
  variant of: http://identifiers.org/hgnc/9955
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11643
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2534
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg171Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

11-65427197-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427197
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427197
    reference: chr 11
allele count: 1
allele frequency: 8.283768783445716e-6
allele num: 120718
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.407G>C
  hgvsp: ENSP00000437137.1:p.Gly136Ala
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.350G>C
  hgvsp: ENSP00000432922.1:p.Gly117Ala
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431304
  ensembl transcript: ENST00000526257
  gene symbol: RELA
  hgvsc: ENST00000526257.1:c.18G>C
  hgvsp: ENSP00000431304.1:p.Asp7His
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*197G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.440G>C
  hgvsp: ENSP00000431153.1:p.Gly147Ala
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.499G>C
  hgvsp: ENSP00000432537.1:p.Asp167His
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.437G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.683G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.472G>C
  hgvsp: ENSP00000434372.1:p.Asp158His
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.*63G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.499G>C
  hgvsp: ENSP00000435290.1:p.Asp167His
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.406G>C
  hgvsp: ENSP00000436545.1:p.Asp136His
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.741G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.532G>C
  hgvsp: ENSP00000433526.1:p.Asp178His
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.499G>C
  hgvsp: ENSP00000384273.3:p.Asp167His
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.490G>C
  hgvsp: ENSP00000311508.9:p.Asp164His
  variant of: http://identifiers.org/hgnc/9955
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp167His
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

11-65427199-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427199
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427199
    reference: chr 11
allele count: 1
allele frequency: 8.282670995742708e-6
allele num: 120734
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.681G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.348G>A
  hgvsp: ENST00000527909.1:c.348G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.530G>A
  hgvsp: ENSP00000433526.1:p.Arg177Gln
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.497G>A
  hgvsp: ENSP00000384273.3:p.Arg166Gln
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.435G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*195G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.438G>A
  hgvsp: ENST00000532879.1:c.438G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.488G>A
  hgvsp: ENSP00000311508.9:p.Arg163Gln
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.497G>A
  hgvsp: ENSP00000435290.1:p.Arg166Gln
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.497G>A
  hgvsp: ENSP00000432537.1:p.Arg166Gln
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.404G>A
  hgvsp: ENSP00000436545.1:p.Arg135Gln
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431304
  ensembl transcript: ENST00000526257
  gene symbol: RELA
  hgvsc: ENST00000526257.1:c.16G>A
  hgvsp: ENSP00000431304.1:p.Arg6Gln
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.405G>A
  hgvsp: ENST00000529389.1:c.405G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.*61G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.470G>A
  hgvsp: ENSP00000434372.1:p.Arg157Gln
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.739G>A
  variant of: http://identifiers.org/hgnc/9955
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11912
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31180
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg166Gln
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: African
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD

11-65427200-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427200
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427200
    reference: chr 11
allele count: 1
allele frequency: 8.279653579294243e-6
allele num: 120778
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431304
  ensembl transcript: ENST00000526257
  gene symbol: RELA
  hgvsc: ENST00000526257.1:c.15C>T
  hgvsp: ENSP00000431304.1:p.Arg6Trp
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.487C>T
  hgvsp: ENSP00000311508.9:p.Arg163Trp
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*194C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.404C>T
  hgvsp: ENSP00000437137.1:p.Ala135Val
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.469C>T
  hgvsp: ENSP00000434372.1:p.Arg157Trp
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.347C>T
  hgvsp: ENSP00000432922.1:p.Ala116Val
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.738C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.529C>T
  hgvsp: ENSP00000433526.1:p.Arg177Trp
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.496C>T
  hgvsp: ENSP00000435290.1:p.Arg166Trp
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.403C>T
  hgvsp: ENSP00000436545.1:p.Arg135Trp
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.496C>T
  hgvsp: ENSP00000432537.1:p.Arg166Trp
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.437C>T
  hgvsp: ENSP00000431153.1:p.Ala146Val
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.680C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.434C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.*60C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.496C>T
  hgvsp: ENSP00000384273.3:p.Arg166Trp
  variant of: http://identifiers.org/hgnc/9955
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12218
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31196
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg166Trp
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

11-65427201-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427201
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427201
    reference: chr 11
allele count: 35
allele frequency: 2.897303024784358e-4
allele num: 120802
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.346G>A
  hgvsp: ENSP00000432922.1:p.Ala116Thr
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.528G>A
  hgvsp: ENST00000532999.1:c.528G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431304
  ensembl transcript: ENST00000526257
  gene symbol: RELA
  hgvsc: ENST00000526257.1:c.14G>A
  hgvsp: ENST00000526257.1:c.14G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.737G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.495G>A
  hgvsp: ENST00000406246.3:c.495G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.433G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.402G>A
  hgvsp: ENST00000527749.1:c.402G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.403G>A
  hgvsp: ENSP00000437137.1:p.Ala135Thr
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.495G>A
  hgvsp: ENST00000525693.1:c.495G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.436G>A
  hgvsp: ENSP00000431153.1:p.Ala146Thr
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.*59G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.495G>A
  hgvsp: ENST00000526283.2:c.495G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.468G>A
  hgvsp: ENST00000534558.1:c.468G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.486G>A
  hgvsp: ENST00000308639.9:c.486G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*193G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.679G>A
  variant of: http://identifiers.org/hgnc/9955
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala146Thr
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

11-65427223-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427223
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427223
    reference: chr 11
allele count: 2
allele frequency: 1.655327672112695e-5
allele num: 120822
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.446G>A
  hgvsp: ENSP00000434372.1:p.Arg149Gln
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*171G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.324G>A
  hgvsp: ENST00000527909.1:c.324G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.380G>A
  hgvsp: ENSP00000436545.1:p.Arg127Gln
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.411G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.*37G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.473G>A
  hgvsp: ENSP00000432537.1:p.Arg158Gln
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.657G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.464G>A
  hgvsp: ENSP00000311508.9:p.Arg155Gln
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.506G>A
  hgvsp: ENSP00000433526.1:p.Arg169Gln
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.473G>A
  hgvsp: ENSP00000384273.3:p.Arg158Gln
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*199G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.473G>A
  hgvsp: ENSP00000435290.1:p.Arg158Gln
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.428-14G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.715G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.381G>A
  hgvsp: ENST00000529389.1:c.381G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2513
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg158Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

11-65427228-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427228
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427228
    reference: chr 11
allele count: 3
allele frequency: 2.484636663298604e-5
allele num: 120742
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.459T>C
  hgvsp: ENST00000308639.9:c.459T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.710T>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.441T>C
  hgvsp: ENST00000534558.1:c.441T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.376T>C
  hgvsp: ENSP00000437137.1:p.Cys126Arg
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.652T>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.501T>C
  hgvsp: ENST00000532999.1:c.501T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.468T>C
  hgvsp: ENST00000525693.1:c.468T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.428-19T>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.319T>C
  hgvsp: ENSP00000432922.1:p.Cys107Arg
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.468T>C
  hgvsp: ENST00000526283.2:c.468T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*194T>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.*32T>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*166T>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.375T>C
  hgvsp: ENST00000527749.1:c.375T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.468T>C
  hgvsp: ENST00000406246.3:c.468T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.406T>C
  variant of: http://identifiers.org/hgnc/9955
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12106
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31207
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys126Arg
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

11-65427237-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427237
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427237
    reference: chr 11
allele count: 1
allele frequency: 8.299306178003518e-6
allele num: 120492
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.459C>T
  hgvsp: ENST00000526283.2:c.459C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.432C>T
  hgvsp: ENST00000534558.1:c.432C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.310C>T
  hgvsp: ENSP00000432922.1:p.Pro104Ser
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*185C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.366C>T
  hgvsp: ENST00000527749.1:c.366C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.643C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.367C>T
  hgvsp: ENSP00000437137.1:p.Pro123Ser
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.450C>T
  hgvsp: ENST00000308639.9:c.450C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.459C>T
  hgvsp: ENST00000406246.3:c.459C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.701C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.459C>T
  hgvsp: ENST00000525693.1:c.459C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.*23C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.428-28C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*157C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.492C>T
  hgvsp: ENST00000532999.1:c.492C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.397C>T
  variant of: http://identifiers.org/hgnc/9955
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro123Ser
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

11-65427240-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427240
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427240
    reference: chr 11
allele count: 78
allele frequency: 6.481527646208307e-4
allele num: 120342
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.456C>T
  hgvsp: ENST00000526283.2:c.456C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.364C>T
  hgvsp: ENSP00000437137.1:p.Arg122Ter
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.*20C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.698C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.456C>T
  hgvsp: ENST00000406246.3:c.456C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.640C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*154C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.456C>T
  hgvsp: ENST00000525693.1:c.456C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.429C>T
  hgvsp: ENST00000534558.1:c.429C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.447C>T
  hgvsp: ENST00000308639.9:c.447C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.363C>T
  hgvsp: ENST00000527749.1:c.363C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*182C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.489C>T
  hgvsp: ENST00000532999.1:c.489C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.307C>T
  hgvsp: ENSP00000432922.1:p.Arg103Ter
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.394C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.428-31C>T
  variant of: http://identifiers.org/hgnc/9955
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 4.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg122Ter
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

11-65427246-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427246
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427246
    reference: chr 11
allele count: 1
allele frequency: 8.347942232239753e-6
allele num: 119790
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.692G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*148G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.358G>A
  hgvsp: ENSP00000437137.1:p.Gly120Arg
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.450G>A
  hgvsp: ENST00000406246.3:c.450G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.*14G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.634G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.441G>A
  hgvsp: ENST00000308639.9:c.441G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.450G>A
  hgvsp: ENST00000525693.1:c.450G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.428-37G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.450G>A
  hgvsp: ENST00000526283.2:c.450G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.357G>A
  hgvsp: ENST00000527749.1:c.357G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.301G>A
  hgvsp: ENSP00000432922.1:p.Gly101Arg
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.483G>A
  hgvsp: ENST00000532999.1:c.483G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.423G>A
  hgvsp: ENST00000534558.1:c.423G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*176G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.388G>A
  variant of: http://identifiers.org/hgnc/9955
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30595
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly120Arg
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

11-65427250-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427250
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427250
    reference: chr 11
allele count: 4
allele frequency: 3.351094132234175e-5
allele num: 119364
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.419G>A
  hgvsp: ENSP00000434372.1:p.Arg140His
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.479G>A
  hgvsp: ENSP00000433526.1:p.Arg160His
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.*10G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.354G>A
  hgvsp: ENST00000529389.1:c.354G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*172G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.384G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.446G>A
  hgvsp: ENSP00000435290.1:p.Arg149His
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.446G>A
  hgvsp: ENSP00000384273.3:p.Arg149His
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.446G>A
  hgvsp: ENSP00000432537.1:p.Arg149His
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*144G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.353G>A
  hgvsp: ENSP00000436545.1:p.Arg118His
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.688G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.428-41G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.297G>A
  hgvsp: ENST00000527909.1:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.437G>A
  hgvsp: ENSP00000311508.9:p.Arg146His
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.630G>A
  variant of: http://identifiers.org/hgnc/9955
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg149His
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: C
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

11-65427271-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427271
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427271
    reference: chr 11
allele count: 1
allele frequency: 8.560764305037153e-6
allele num: 116812
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.612-3C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.670-3C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.428-12C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.187-3C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.401-3C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.336-3C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.428-3C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.363C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*126-3C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.279-3C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*154-3C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.461-3C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.335-3C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.428-3C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.428-3C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.428-62C>T
  variant of: http://identifiers.org/hgnc/9955
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10446
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11151
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27687
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.428-3C>T
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD

11-65427275-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427275
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427275
    reference: chr 11
allele count: 3
allele frequency: 2.585048081894323e-5
allele num: 116052
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.428-16T>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.401-7T>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*154-7T>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.336-7T>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.461-7T>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.428-7T>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.428-7T>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.335-7T>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.428-7T>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.612-7T>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.670-7T>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*126-7T>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.359T>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.279-7T>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.428-66T>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.187-7T>C
  variant of: http://identifiers.org/hgnc/9955
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2481
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26567
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: c.428-7T>C
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD

11-65427285-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427285
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427285
    reference: chr 11
allele count: 3
allele frequency: 2.62614237193179e-5
allele num: 114236
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.336-17G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.279-17G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.670-17G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.428-76G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.428-17G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*154-17G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.428-17G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.428-26G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.612-17G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.349G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.401-17G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.335-17G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.461-17G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.428-17G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*126-17G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.187-17G>A
  variant of: http://identifiers.org/hgnc/9955
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8207
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2030
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10455
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3061
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8442
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

11-65427286-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427286
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427286
    reference: chr 11
allele count: 3
allele frequency: 2.62894999737105e-5
allele num: 114114
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.401-18C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.670-18C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.428-18C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.348C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.335-18C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.336-18C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.187-18C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.461-18C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.428-27C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.428-18C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*126-18C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.612-18C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.279-18C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*154-18C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.428-18C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.428-77C>T
  variant of: http://identifiers.org/hgnc/9955
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8136
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1999
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3176
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8814
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum

11-65427291-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427291
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427291
    reference: chr 11
allele count: 1
allele frequency: 8.839232047519711e-6
allele num: 113132
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.428-32C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.670-23C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.343C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.187-23C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.335-23C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.279-23C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.401-23C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.428-23C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.428-23C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.428-82C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.336-23C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*126-23C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*154-23C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.461-23C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.428-23C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.612-23C>T
  variant of: http://identifiers.org/hgnc/9955
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9549
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5671
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20004
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3470
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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: G
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff

11-65427296-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427296
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427296
    reference: chr 11
allele count: 1
allele frequency: 8.865877012554082e-6
allele num: 112792
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.428-28C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.428-28C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.428-37C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.336-28C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.670-28C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.401-28C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.335-28C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.428-87C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.461-28C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.187-28C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*154-28C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.338C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.279-28C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.428-28C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.612-28C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*126-28C>G
  variant of: http://identifiers.org/hgnc/9955
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11331
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

11-65427316-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427316
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427316
    reference: chr 11
allele count: 1
allele frequency: 9.215570628133294e-6
allele num: 108512
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*154-48C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.318C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.401-48C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.670-48C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.428-48C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.428-48C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.461-48C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.612-48C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*126-48C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.428-57C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.187-48C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.335-48C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.428-48C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.336-48C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.428-107C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.279-48C>G
  variant of: http://identifiers.org/hgnc/9955
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5205
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12718
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14571
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

11-65427545-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427545
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427545
    reference: chr 11
allele count: 1
allele frequency: 8.246198502490351e-6
allele num: 121268
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000527074
  gene symbol: RELA
  hgvsc: ENST00000527074.1:n.563G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.400+50G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.611+50G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*153+50G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.427+50G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.460+50G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.89G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.427+50G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.669+50G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.187-277G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.427+50G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.336-277G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.427+50G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*125+50G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.334+50G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.278+50G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.427+50G>C
  variant of: http://identifiers.org/hgnc/9955
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1731
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4666
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14107
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff

11-65427545-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427545
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427545
    reference: chr 11
allele count: 1
allele frequency: 8.246198502490351e-6
allele num: 121268
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.336-277G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.427+50G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.427+50G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000527074
  gene symbol: RELA
  hgvsc: ENST00000527074.1:n.563G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.427+50G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*153+50G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.669+50G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.460+50G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.89G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.611+50G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.400+50G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.427+50G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.334+50G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.278+50G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.187-277G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*125+50G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.427+50G>A
  variant of: http://identifiers.org/hgnc/9955
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14107
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2812
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4666
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 1.75e1
  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: African
population: Other
reference allele: C
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

11-65427548-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427548
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427548
    reference: chr 11
allele count: 1
allele frequency: 8.243071698237632e-6
allele num: 121314
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.460+47C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000527074
  gene symbol: RELA
  hgvsc: ENST00000527074.1:n.560C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.427+47C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.278+47C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.334+47C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.427+47C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.427+47C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.669+47C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*125+47C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.336-280C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.427+47C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*153+47C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.86C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.427+47C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.400+47C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.187-280C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.611+47C>T
  variant of: http://identifiers.org/hgnc/9955
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS

11-65427549-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427549
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427549
    reference: chr 11
allele count: 1
allele frequency: 8.24279991427488e-6
allele num: 121318
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.427+46C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.427+46C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.334+46C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.187-281C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.400+46C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.427+46C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.336-281C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.85C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.278+46C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*153+46C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*125+46C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.669+46C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000527074
  gene symbol: RELA
  hgvsc: ENST00000527074.1:n.559C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.611+46C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.427+46C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.427+46C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.460+46C>T
  variant of: http://identifiers.org/hgnc/9955
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2804
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5435
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

11-65427560-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427560
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427560
    reference: chr 11
allele count: 13
allele frequency: 1.071316730670974e-4
allele num: 121346
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*125+35C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.336-292C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.400+35C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.427+35C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.611+35C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.427+35C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.669+35C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.427+35C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*153+35C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.74C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.278+35C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000527074
  gene symbol: RELA
  hgvsc: ENST00000527074.1:n.548C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.187-292C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.460+35C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.427+35C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.334+35C>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.427+35C>G
  variant of: http://identifiers.org/hgnc/9955
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14206
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2795
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1721
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum

11-65427562-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427562
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427562
    reference: chr 11
allele count: 2
allele frequency: 1.648098094798602e-5
allele num: 121352
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.400+33C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.460+33C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.669+33C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.187-294C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.336-294C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.427+33C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.427+33C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000527074
  gene symbol: RELA
  hgvsc: ENST00000527074.1:n.546C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*153+33C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.72C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.427+33C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.427+33C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.427+33C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.334+33C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.611+33C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*125+33C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.278+33C>T
  variant of: http://identifiers.org/hgnc/9955
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-65427564-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427564
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427564
    reference: chr 11
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*153+31C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.427+31C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000527074
  gene symbol: RELA
  hgvsc: ENST00000527074.1:n.544C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.70C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.400+31C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.336-296C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*125+31C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.669+31C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.427+31C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.187-296C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.427+31C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.278+31C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.460+31C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.611+31C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.334+31C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.427+31C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.427+31C>T
  variant of: http://identifiers.org/hgnc/9955
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4831
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2791
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

11-65427567-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427567
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427567
    reference: chr 11
allele count: 1
allele frequency: 8.241441263248117e-6
allele num: 121338
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000527074
  gene symbol: RELA
  hgvsc: ENST00000527074.1:n.541G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.669+28G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.334+28G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.460+28G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.427+28G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.400+28G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.278+28G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.427+28G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.336-299G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.187-299G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.427+28G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.427+28G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.611+28G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.427+28G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*153+28G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.67G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*125+28G>A
  variant of: http://identifiers.org/hgnc/9955
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20496
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2793
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

11-65427568-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427568
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427568
    reference: chr 11
allele count: 9533
allele frequency: 7.857472552833734e-2
allele num: 121324
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.400+27C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.427+27C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.187-300C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.427+27C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.278+27C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.336-300C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.669+27C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000527074
  gene symbol: RELA
  hgvsc: ENST00000527074.1:n.540C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.427+27C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*153+27C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.334+27C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.66C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.427+27C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.611+27C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.427+27C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.460+27C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*125+27C>T
  variant of: http://identifiers.org/hgnc/9955
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4739
  bin: 9.75e1
  variant carriers: 3587
genotype depth: GenotypeDepth
  all individuals: 2688
  bin: 4.25e1
  variant carriers: 304
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 7.75e1
  variant carriers: 540
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 5.25e1
  variant carriers: 347
genotype depth: GenotypeDepth
  all individuals: 20313
  bin: 2.75e1
  variant carriers: 162
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 490
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD

11-65427572-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427572
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427572
    reference: chr 11
allele count: 2
allele frequency: 1.648125257519571e-5
allele num: 121350
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000527074
  gene symbol: RELA
  hgvsc: ENST00000527074.1:n.536C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.400+23C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.427+23C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.62C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.336-304C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.611+23C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.427+23C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.427+23C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*153+23C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*125+23C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.427+23C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.334+23C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.460+23C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.427+23C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.278+23C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.669+23C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.187-304C>T
  variant of: http://identifiers.org/hgnc/9955
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16155
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5269
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

11-65427580-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427580
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427580
    reference: chr 11
allele count: 47
allele frequency: 3.932527862378259e-4
allele num: 119516
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.334+15G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000527074
  gene symbol: RELA
  hgvsc: ENST00000527074.1:n.528G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.400+15G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.427+15G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.336-312G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.54G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.427+15G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.427+15G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.427+15G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.669+15G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.278+15G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*125+15G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.427+15G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.187-312G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*153+15G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.611+15G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.460+15G>C
  variant of: http://identifiers.org/hgnc/9955
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23950
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum

11-65427581-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427581
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427581
    reference: chr 11
allele count: 11
allele frequency: 9.077555331825909e-5
allele num: 121178
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.278+14T>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.460+14T>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.53T>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*153+14T>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.427+14T>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.427+14T>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.427+14T>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*125+14T>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.427+14T>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.400+14T>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.187-313T>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.336-313T>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.427+14T>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.334+14T>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.669+14T>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000527074
  gene symbol: RELA
  hgvsc: ENST00000527074.1:n.527T>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.611+14T>C
  variant of: http://identifiers.org/hgnc/9955
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2802
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1426
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

11-65427583-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427583
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427582
    reference: chr 11
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.427+11delA
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.336-316delA
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.187-316delA
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.427+11delA
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*125+11delA
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.427+11delA
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.460+11delA
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.334+11delA
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.278+11delA
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.611+11delA
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*153+11delA
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000527074
  gene symbol: RELA
  hgvsc: ENST00000527074.1:n.524delA
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.669+11delA
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.427+11delA
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.427+11delA
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.400+11delA
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.50delA
  variant of: http://identifiers.org/hgnc/9955
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6031
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16498
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2811
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: GT
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

11-65427584-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427584
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427584
    reference: chr 11
allele count: 70
allele frequency: 5.820044232336166e-4
allele num: 120274
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*125+11A>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.427+11A>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.427+11A>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.50A>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.427+11A>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000527074
  gene symbol: RELA
  hgvsc: ENST00000527074.1:n.524A>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.460+11A>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.187-316A>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.427+11A>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.611+11A>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*153+11A>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.336-316A>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.400+11A>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.278+11A>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.427+11A>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.669+11A>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.334+11A>C
  variant of: http://identifiers.org/hgnc/9955
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 4.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 5.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 7.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

11-65427606-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427606
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427606
    reference: chr 11
allele count: 34
allele frequency: 2.812195000909828e-4
allele num: 120902
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.658A>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.416A>C
  hgvsp: ENSP00000432537.1:p.Asn139Thr
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*114A>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.389A>C
  hgvsp: ENSP00000434372.1:p.Asn130Thr
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.600A>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.416A>C
  hgvsp: ENSP00000311508.9:p.Asn139Thr
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.187-338A>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.416A>C
  hgvsp: ENSP00000384273.3:p.Asn139Thr
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.416A>C
  hgvsp: ENSP00000431153.1:p.Asn139Thr
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.323A>C
  hgvsp: ENSP00000436545.1:p.Asn108Thr
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.267A>C
  hgvsp: ENSP00000432922.1:p.Gln89His
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.28A>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.336-338A>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000527074
  gene symbol: RELA
  hgvsc: ENST00000527074.1:n.502A>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.449A>C
  hgvsp: ENSP00000433526.1:p.Asn150Thr
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*142A>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.416A>C
  hgvsp: ENSP00000435290.1:p.Asn139Thr
  variant of: http://identifiers.org/hgnc/9955
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn139Thr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

11-65427616-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427616
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427616
    reference: chr 11
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*104A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.590A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.648A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.18A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.313A>G
  hgvsp: ENSP00000436545.1:p.Thr105Ala
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.406A>G
  hgvsp: ENSP00000311508.9:p.Thr136Ala
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.406A>G
  hgvsp: ENSP00000384273.3:p.Thr136Ala
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.406A>G
  hgvsp: ENSP00000435290.1:p.Thr136Ala
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.187-348A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.406A>G
  hgvsp: ENSP00000431153.1:p.Thr136Ala
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.379A>G
  hgvsp: ENSP00000434372.1:p.Thr127Ala
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.439A>G
  hgvsp: ENSP00000433526.1:p.Thr147Ala
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.336-348A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000527074
  gene symbol: RELA
  hgvsc: ENST00000527074.1:n.492A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.257A>G
  hgvsp: ENSP00000432922.1:p.Asp86Gly
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.406A>G
  hgvsp: ENSP00000432537.1:p.Thr136Ala
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*132A>G
  variant of: http://identifiers.org/hgnc/9955
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr136Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: T
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

11-65427617-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427617
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427617
    reference: chr 11
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.405G>C
  hgvsp: ENSP00000432537.1:p.Gln135His
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000527074
  gene symbol: RELA
  hgvsc: ENST00000527074.1:n.491G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.187-349G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.438G>C
  hgvsp: ENSP00000433526.1:p.Gln146His
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.405G>C
  hgvsp: ENSP00000431153.1:p.Gln135His
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.589G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.405G>C
  hgvsp: ENSP00000384273.3:p.Gln135His
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.378G>C
  hgvsp: ENSP00000434372.1:p.Gln126His
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.405G>C
  hgvsp: ENSP00000311508.9:p.Gln135His
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.312G>C
  hgvsp: ENSP00000436545.1:p.Gln104His
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*131G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.647G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.405G>C
  hgvsp: ENSP00000435290.1:p.Gln135His
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.336-349G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.256G>C
  hgvsp: ENSP00000432922.1:p.Asp86His
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.17G>C
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*103G>C
  variant of: http://identifiers.org/hgnc/9955
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln135His
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ

11-65427624-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427624
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427624
    reference: chr 11
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000527074
  gene symbol: RELA
  hgvsc: ENST00000527074.1:n.484G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.431G>A
  hgvsp: ENSP00000433526.1:p.Arg144His
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.305G>A
  hgvsp: ENSP00000436545.1:p.Arg102His
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*96G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.336-356G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.398G>A
  hgvsp: ENSP00000432537.1:p.Arg133His
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.398G>A
  hgvsp: ENSP00000384273.3:p.Arg133His
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.398G>A
  hgvsp: ENSP00000311508.9:p.Arg133His
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*124G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.249G>A
  hgvsp: ENST00000527909.1:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.398G>A
  hgvsp: ENSP00000435290.1:p.Arg133His
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.582G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.640G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.187-356G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.371G>A
  hgvsp: ENSP00000434372.1:p.Arg124His
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000529330
  gene symbol: RELA
  hgvsc: ENST00000529330.1:n.10G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.398G>A
  hgvsp: ENSP00000431153.1:p.Arg133His
  variant of: http://identifiers.org/hgnc/9955
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25100
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg133His
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

11-65427647-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427647
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427647
    reference: chr 11
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.336-379C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.375C>T
  hgvsp: ENST00000406246.3:c.375C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.375C>T
  hgvsp: ENST00000526283.2:c.375C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.375C>T
  hgvsp: ENST00000525693.1:c.375C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.226C>T
  hgvsp: ENSP00000432922.1:p.Pro76Ser
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.375C>T
  hgvsp: ENST00000532879.1:c.375C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*101C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.348C>T
  hgvsp: ENST00000534558.1:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.559C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.375C>T
  hgvsp: ENST00000308639.9:c.375C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.282C>T
  hgvsp: ENST00000527749.1:c.282C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000525301
  gene symbol: RELA
  hgvsc: ENST00000525301.1:n.603C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000527074
  gene symbol: RELA
  hgvsc: ENST00000527074.1:n.461C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.617C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434098
  ensembl transcript: ENST00000533187
  gene symbol: RELA
  hgvsc: ENST00000533187.1:c.282C>T
  hgvsp: ENST00000533187.1:c.282C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.408C>T
  hgvsp: ENST00000532999.1:c.408C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.187-379C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*73C>T
  variant of: http://identifiers.org/hgnc/9955
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro76Ser
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD

11-65427651-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427651
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427651
    reference: chr 11
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.371G>A
  hgvsp: ENSP00000431153.1:p.Arg124Gln
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.555G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.404G>A
  hgvsp: ENSP00000433526.1:p.Arg135Gln
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.371G>A
  hgvsp: ENSP00000435290.1:p.Arg124Gln
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.187-383G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.371G>A
  hgvsp: ENSP00000384273.3:p.Arg124Gln
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000527074
  gene symbol: RELA
  hgvsc: ENST00000527074.1:n.457G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.371G>A
  hgvsp: ENSP00000311508.9:p.Arg124Gln
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.371G>A
  hgvsp: ENSP00000432537.1:p.Arg124Gln
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.222G>A
  hgvsp: ENST00000527909.1:c.222G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.278G>A
  hgvsp: ENSP00000436545.1:p.Arg93Gln
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.336-383G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.344G>A
  hgvsp: ENSP00000434372.1:p.Arg115Gln
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434098
  ensembl transcript: ENST00000533187
  gene symbol: RELA
  hgvsc: ENST00000533187.1:c.278G>A
  hgvsp: ENSP00000434098.1:p.Arg93Gln
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.613G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*97G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000525301
  gene symbol: RELA
  hgvsc: ENST00000525301.1:n.599G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*69G>A
  variant of: http://identifiers.org/hgnc/9955
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg124Gln
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ

11-65427654-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427654
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427654
    reference: chr 11
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.368A>G
  hgvsp: ENSP00000432537.1:p.Lys123Arg
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*66A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.341A>G
  hgvsp: ENSP00000434372.1:p.Lys114Arg
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.401A>G
  hgvsp: ENSP00000433526.1:p.Lys134Arg
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.552A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.187-386A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.219A>G
  hgvsp: ENST00000527909.1:c.219A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000527074
  gene symbol: RELA
  hgvsc: ENST00000527074.1:n.454A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.610A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.368A>G
  hgvsp: ENSP00000435290.1:p.Lys123Arg
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*94A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.336-386A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.275A>G
  hgvsp: ENSP00000436545.1:p.Lys92Arg
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434098
  ensembl transcript: ENST00000533187
  gene symbol: RELA
  hgvsc: ENST00000533187.1:c.275A>G
  hgvsp: ENSP00000434098.1:p.Lys92Arg
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.368A>G
  hgvsp: ENSP00000311508.9:p.Lys123Arg
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000525301
  gene symbol: RELA
  hgvsc: ENST00000525301.1:n.596A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.368A>G
  hgvsp: ENSP00000431153.1:p.Lys123Arg
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.368A>G
  hgvsp: ENSP00000384273.3:p.Lys123Arg
  variant of: http://identifiers.org/hgnc/9955
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5606
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys123Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

11-65427671-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427671
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427671
    reference: chr 11
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.351A>G
  hgvsp: ENST00000525693.1:c.351A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.384A>G
  hgvsp: ENST00000532999.1:c.384A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.351A>G
  hgvsp: ENST00000532879.1:c.351A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.324A>G
  hgvsp: ENST00000534558.1:c.324A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000525301
  gene symbol: RELA
  hgvsc: ENST00000525301.1:n.579A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.351A>G
  hgvsp: ENST00000308639.9:c.351A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434098
  ensembl transcript: ENST00000533187
  gene symbol: RELA
  hgvsc: ENST00000533187.1:c.258A>G
  hgvsp: ENST00000533187.1:c.258A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.336-403A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*77A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435531
  ensembl transcript: ENST00000527874
  gene symbol: RELA
  hgvsc: ENST00000527874.1:c.258A>G
  hgvsp: ENST00000527874.1:c.258A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.258A>G
  hgvsp: ENST00000527749.1:c.258A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.351A>G
  hgvsp: ENST00000406246.3:c.351A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.535A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.593A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.202A>G
  hgvsp: ENSP00000432922.1:p.Asn68Asp
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.187-403A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*49A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.351A>G
  hgvsp: ENST00000526283.2:c.351A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000527074
  gene symbol: RELA
  hgvsc: ENST00000527074.1:n.437A>G
  variant of: http://identifiers.org/hgnc/9955
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asn68Asp
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

11-65427689-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427689
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427689
    reference: chr 11
allele count: 1
allele frequency: 8.254366559910193e-6
allele num: 121148
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.336-421C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.336-3C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.520-3C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000525301
  gene symbol: RELA
  hgvsc: ENST00000525301.1:n.564-3C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.336-3C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.309-3C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.336-3C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.243-3C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.187-3C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.336-3C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*62-3C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*34-3C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435531
  ensembl transcript: ENST00000527874
  gene symbol: RELA
  hgvsc: ENST00000527874.1:c.243-3C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000527074
  gene symbol: RELA
  hgvsc: ENST00000527074.1:n.422-3C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.336-3C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.369-3C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.575C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434098
  ensembl transcript: ENST00000533187
  gene symbol: RELA
  hgvsc: ENST00000533187.1:c.243-3C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.187-421C>T
  variant of: http://identifiers.org/hgnc/9955
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.336-3C>T
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: G
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD

11-65427692-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427692
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427692
    reference: chr 11
allele count: 1
allele frequency: 8.271982794275789e-6
allele num: 120890
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*62-6G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.243-6G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.187-6G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.336-6G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.572G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.309-6G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.336-6G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.336-6G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.336-6G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.187-424G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434098
  ensembl transcript: ENST00000533187
  gene symbol: RELA
  hgvsc: ENST00000533187.1:c.243-6G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*34-6G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.520-6G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435531
  ensembl transcript: ENST00000527874
  gene symbol: RELA
  hgvsc: ENST00000527874.1:c.243-6G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000527074
  gene symbol: RELA
  hgvsc: ENST00000527074.1:n.422-6G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.336-424G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000525301
  gene symbol: RELA
  hgvsc: ENST00000525301.1:n.564-6G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.369-6G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.336-6G>A
  variant of: http://identifiers.org/hgnc/9955
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.336-6G>A
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

11-65427693-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427693
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427693
    reference: chr 11
allele count: 9
allele frequency: 7.446139590296852e-5
allele num: 120868
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.336-7C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.520-7C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.336-7C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*34-7C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.187-425C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.336-7C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435531
  ensembl transcript: ENST00000527874
  gene symbol: RELA
  hgvsc: ENST00000527874.1:c.243-7C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.369-7C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.243-7C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.309-7C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.571C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434098
  ensembl transcript: ENST00000533187
  gene symbol: RELA
  hgvsc: ENST00000533187.1:c.243-7C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000525301
  gene symbol: RELA
  hgvsc: ENST00000525301.1:n.564-7C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.187-7C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.336-7C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.336-425C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*62-7C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000527074
  gene symbol: RELA
  hgvsc: ENST00000527074.1:n.422-7C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.336-7C>T
  variant of: http://identifiers.org/hgnc/9955
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.336-7C>T
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

11-65427693-G-GC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427693
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427694
    reference: chr 11
allele count: 1
allele frequency: 8.27348843366317e-6
allele num: 120868
alternate allele: GC
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.336-426dupG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.187-8dupG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*34-8dupG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435531
  ensembl transcript: ENST00000527874
  gene symbol: RELA
  hgvsc: ENST00000527874.1:c.243-8dupG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.309-8dupG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000525301
  gene symbol: RELA
  hgvsc: ENST00000525301.1:n.564-8dupG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.336-8dupG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.369-8dupG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434098
  ensembl transcript: ENST00000533187
  gene symbol: RELA
  hgvsc: ENST00000533187.1:c.243-8dupG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.336-8dupG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.336-8dupG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.520-8dupG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000527074
  gene symbol: RELA
  hgvsc: ENST00000527074.1:n.422-8dupG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.187-426dupG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*62-8dupG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.336-8dupG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.243-8dupG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.336-8dupG
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.570dupG
  variant of: http://identifiers.org/hgnc/9955
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.336-8dupG
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD

11-65427695-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427695
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427695
    reference: chr 11
allele count: 1
allele frequency: 8.27787159365584e-6
allele num: 120804
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.309-9G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.187-427G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*34-9G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.336-9G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.569G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.336-427G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435531
  ensembl transcript: ENST00000527874
  gene symbol: RELA
  hgvsc: ENST00000527874.1:c.243-9G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434098
  ensembl transcript: ENST00000533187
  gene symbol: RELA
  hgvsc: ENST00000533187.1:c.243-9G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.336-9G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.336-9G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.520-9G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.336-9G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*62-9G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.336-9G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.243-9G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.369-9G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000525301
  gene symbol: RELA
  hgvsc: ENST00000525301.1:n.564-9G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.187-9G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000527074
  gene symbol: RELA
  hgvsc: ENST00000527074.1:n.422-9G>A
  variant of: http://identifiers.org/hgnc/9955
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: South Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/11-65427702-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427702
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427702
    reference: chr 11
allele count: 1
allele frequency: 8.299306178003518e-6
allele num: 120492
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.187-16G>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.187-434G>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000527074
  gene symbol: RELA
  hgvsc: ENST00000527074.1:n.422-16G>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.336-16G>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.336-16G>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*62-16G>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434098
  ensembl transcript: ENST00000533187
  gene symbol: RELA
  hgvsc: ENST00000533187.1:c.243-16G>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435531
  ensembl transcript: ENST00000527874
  gene symbol: RELA
  hgvsc: ENST00000527874.1:c.243-16G>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.336-16G>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.336-434G>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.369-16G>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.562G>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.309-16G>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.243-16G>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.336-16G>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000525301
  gene symbol: RELA
  hgvsc: ENST00000525301.1:n.564-16G>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*34-16G>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.520-16G>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.336-16G>T
  variant of: http://identifiers.org/hgnc/9955
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

11-65427702-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427702
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427702
    reference: chr 11
allele count: 4
allele frequency: 3.319722471201407e-5
allele num: 120492
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.187-434G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.187-16G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.309-16G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435531
  ensembl transcript: ENST00000527874
  gene symbol: RELA
  hgvsc: ENST00000527874.1:c.243-16G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000525301
  gene symbol: RELA
  hgvsc: ENST00000525301.1:n.564-16G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*34-16G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.562G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.336-16G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*62-16G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434098
  ensembl transcript: ENST00000533187
  gene symbol: RELA
  hgvsc: ENST00000533187.1:c.243-16G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.336-16G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.336-434G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.336-16G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.336-16G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.336-16G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000527074
  gene symbol: RELA
  hgvsc: ENST00000527074.1:n.422-16G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.369-16G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.520-16G>A
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.243-16G>A
  variant of: http://identifiers.org/hgnc/9955
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

11-65427703-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427703
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427703
    reference: chr 11
allele count: 1
allele frequency: 8.302613662781043e-6
allele num: 120444
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.561C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.187-435C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.336-17C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.336-17C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.369-17C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.520-17C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*62-17C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*34-17C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434098
  ensembl transcript: ENST00000533187
  gene symbol: RELA
  hgvsc: ENST00000533187.1:c.243-17C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435531
  ensembl transcript: ENST00000527874
  gene symbol: RELA
  hgvsc: ENST00000527874.1:c.243-17C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.336-17C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.309-17C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.336-435C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.187-17C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.243-17C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.336-17C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000527074
  gene symbol: RELA
  hgvsc: ENST00000527074.1:n.422-17C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000525301
  gene symbol: RELA
  hgvsc: ENST00000525301.1:n.564-17C>T
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.336-17C>T
  variant of: http://identifiers.org/hgnc/9955
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD

11-65427706-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65427706
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 65427706
    reference: chr 11
allele count: 1
allele frequency: 8.316561600771776e-6
allele num: 120242
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434745
  ensembl transcript: ENST00000531238
  gene symbol: RELA
  hgvsc: ENST00000531238.1:c.*62-20A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433144
  ensembl transcript: ENST00000533546
  gene symbol: RELA
  hgvsc: ENST00000533546.1:c.187-438A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000527074
  gene symbol: RELA
  hgvsc: ENST00000527074.1:n.422-20A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000311508
  ensembl transcript: ENST00000308639
  gene symbol: RELA
  hgvsc: ENST00000308639.9:c.336-20A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000384273
  ensembl transcript: ENST00000406246
  gene symbol: RELA
  hgvsc: ENST00000406246.3:c.336-20A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000431153
  ensembl transcript: ENST00000532879
  gene symbol: RELA
  hgvsc: ENST00000532879.1:c.336-20A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000525301
  gene symbol: RELA
  hgvsc: ENST00000525301.1:n.564-20A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434008
  ensembl transcript: ENST00000525658
  gene symbol: RELA
  hgvsc: ENST00000525658.1:c.*34-20A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434372
  ensembl transcript: ENST00000534558
  gene symbol: RELA
  hgvsc: ENST00000534558.1:c.309-20A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000531484
  gene symbol: RELA
  hgvsc: ENST00000531484.1:n.520-20A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000437137
  ensembl transcript: ENST00000529389
  gene symbol: RELA
  hgvsc: ENST00000529389.1:c.336-438A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000433526
  ensembl transcript: ENST00000532999
  gene symbol: RELA
  hgvsc: ENST00000532999.1:c.369-20A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432537
  ensembl transcript: ENST00000525693
  gene symbol: RELA
  hgvsc: ENST00000525693.1:c.336-20A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000173039
  ensembl transcript: ENST00000526738
  gene symbol: RELA
  hgvsc: ENST00000526738.1:n.558A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000436545
  ensembl transcript: ENST00000527749
  gene symbol: RELA
  hgvsc: ENST00000527749.1:c.243-20A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435531
  ensembl transcript: ENST00000527874
  gene symbol: RELA
  hgvsc: ENST00000527874.1:c.243-20A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000435290
  ensembl transcript: ENST00000526283
  gene symbol: RELA
  hgvsc: ENST00000526283.2:c.336-20A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000434098
  ensembl transcript: ENST00000533187
  gene symbol: RELA
  hgvsc: ENST00000533187.1:c.243-20A>G
  variant of: http://identifiers.org/hgnc/9955
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000173039
  ensembl protein: ENSP00000432922
  ensembl transcript: ENST00000527909
  gene symbol: RELA
  hgvsc: ENST00000527909.1:c.187-20A>G
  variant of: http://identifiers.org/hgnc/9955
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2797
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5101
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
reference allele: T

GenotypeDepth
all individuals: 335
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8501
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 114
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 166
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 57
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1527
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5068
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 134
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 637
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2163
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10443
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1126
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2331
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1321
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7226
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5063
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14279
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4181
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1696
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2001
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3342
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3010
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1177
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 834
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10306
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66214
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16470
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.278e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.981192e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.505e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.33e0

MQRankSum
type: SiteQuality
SIO_000300: -2.67e-1

GenotypeDepth
all individuals: 24
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 637
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 235
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 40
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1859
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13014
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 438
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12601
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 166
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4181
bin: 8.25e1
variant carriers: 0

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

Other
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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South Asian
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.510254628930438e-5
allele num: 66214
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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QD
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FS
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MQRankSum
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MQ
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.630487127245786e-5
allele num: 64788
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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Other
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BaseQRankSum
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SIO_000300: -3.3e-1

InbreedingCoeff
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FS
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ClippingRankSum
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VQSLOD
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QD
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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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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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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
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allele num: 64826
num of homozygotes: 0

Latino
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allele num: 11538
num of homozygotes: 0

East Asian
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South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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Other
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QD
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SIO_000300: 1.507e1

FS
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BaseQRankSum
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SIO_000300: 2.09e-1

ClippingRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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MQRankSum
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DP
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SIO_000300: 1.665879e6

ReadPosRankSum
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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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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 1.214034235765449e-4
allele num: 16474
num of homozygotes: 0

European (Non-Finnish)
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East Asian
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allele num: 8586
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Latino
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Other
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European (Finnish)
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African
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MQRankSum
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QD
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BaseQRankSum
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MQ
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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FS
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DP
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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European (Finnish)
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Other
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South Asian
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Latino
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QD
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MQRankSum
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VQSLOD
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ReadPosRankSum
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FS
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DP
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MQ
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InbreedingCoeff
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ClippingRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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European (Non-Finnish)
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Latino
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South Asian
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European (Finnish)
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MQ
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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MQRankSum
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ClippingRankSum
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FS
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DP
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Latino
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African
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European (Non-Finnish)
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South Asian
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Other
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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DP
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InbreedingCoeff
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MQ
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MQRankSum
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FS
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Finnish)
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Latino
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African
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South Asian
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Other
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East Asian
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MQRankSum
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FS
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DP
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MQ
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QD
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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Other
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South Asian
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East Asian
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European (Finnish)
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ClippingRankSum
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VQSLOD
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QD
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BaseQRankSum
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FS
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MQ
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InbreedingCoeff
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ReadPosRankSum
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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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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Non-Finnish)
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African
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Other
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European (Finnish)
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South Asian
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East Asian
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VQSLOD
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MQ
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FS
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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DP
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BaseQRankSum
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ReadPosRankSum
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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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European (Finnish)
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European (Non-Finnish)
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African
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South Asian
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Latino
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East Asian
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QD
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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FS
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MQ
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BaseQRankSum
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DP
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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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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MQRankSum
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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QD
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FS
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InbreedingCoeff
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ReadPosRankSum
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DP
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MQ
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GenotypeDepth
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GenotypeDepth
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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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Other
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African
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Latino
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South Asian
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East Asian
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European (Finnish)
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InbreedingCoeff
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BaseQRankSum
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MQ
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MQRankSum
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VQSLOD
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FS
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ReadPosRankSum
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ClippingRankSum
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QD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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Other
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Latino
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East Asian
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European (Finnish)
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South Asian
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BaseQRankSum
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MQ
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MQRankSum
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ReadPosRankSum
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QD
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FS
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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South Asian
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European (Finnish)
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African
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Other
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QD
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FS
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InbreedingCoeff
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MQRankSum
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DP
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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East Asian
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European (Non-Finnish)
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European (Finnish)
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Other
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South Asian
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Latino
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African
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MQRankSum
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ReadPosRankSum
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FS
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InbreedingCoeff
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BaseQRankSum
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MQ
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VQSLOD
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DP
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ClippingRankSum
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QD
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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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Other
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European (Non-Finnish)
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South Asian
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Latino
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European (Finnish)
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East Asian
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African
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ReadPosRankSum
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FS
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InbreedingCoeff
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DP
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VQSLOD
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QD
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MQ
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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European (Non-Finnish)
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South Asian
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QD
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DP
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MQ
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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FS
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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South Asian
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MQRankSum
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FS
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BaseQRankSum
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MQ
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InbreedingCoeff
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ClippingRankSum
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QD
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DP
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ReadPosRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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Latino
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East Asian
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European (Finnish)
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European (Non-Finnish)
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Other
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South Asian
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BaseQRankSum
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FS
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ReadPosRankSum
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ClippingRankSum
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QD
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MQRankSum
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VQSLOD
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InbreedingCoeff
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DP
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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Other
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Latino
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East Asian
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European (Non-Finnish)
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South Asian
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European (Finnish)
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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FS
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VQSLOD
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QD
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InbreedingCoeff
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DP
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MQ
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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European (Non-Finnish)
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East Asian
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African
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Other
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MQ
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MQRankSum
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BaseQRankSum
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FS
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InbreedingCoeff
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QD
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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DP
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European (Non-Finnish)
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African
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Other
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South Asian
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Latino
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East Asian
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FS
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MQRankSum
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DP
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ReadPosRankSum
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InbreedingCoeff
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QD
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MQ
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Non-Finnish)
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African
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East Asian
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Latino
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South Asian
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allele num: 15696
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European (Finnish)
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allele frequency: 0.0e0
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MQRankSum
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QD
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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FS
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MQ
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DP
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BaseQRankSum
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ClippingRankSum
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SIO_000300: -8.44e-1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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Other
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.538508877196221e-5
allele num: 64998
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BaseQRankSum
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SIO_000300: -1.713e0

MQRankSum
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ClippingRankSum
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QD
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ReadPosRankSum
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MQ
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InbreedingCoeff
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FS
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DP
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VQSLOD
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GenotypeDepth
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variant carriers: 1

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

East Asian
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allele count: 3
allele frequency: 3.524436090225564e-4
allele num: 8512
num of homozygotes: 0

South Asian
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MQRankSum
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SIO_000300: -4.87e-1

FS
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MQ
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SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: 7.15e-1

ClippingRankSum
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SIO_000300: 2.25e-1

InbreedingCoeff
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VQSLOD
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DP
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

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

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

African
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Latino
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South Asian
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European (Non-Finnish)
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European (Finnish)
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Other
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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VQSLOD
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QD
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InbreedingCoeff
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DP
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FS
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MQ
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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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European (Finnish)
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allele count: 0
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South Asian
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Latino
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East Asian
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African
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Other
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European (Non-Finnish)
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MQRankSum
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SIO_000300: 2.6e-1

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

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

African
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allele frequency: 0.0e0
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East Asian
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Latino
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allele frequency: 1.728011059270779e-4
allele num: 11574
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: 66692
num of homozygotes: 0

Other
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InbreedingCoeff
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VQSLOD
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DP
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MQ
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QD
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FS
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BaseQRankSum
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MQRankSum
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SIO_000300: 1.73e0

ClippingRankSum
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ReadPosRankSum
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SIO_000300: -4.18e-1

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
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allele num: 66694
num of homozygotes: 0

South Asian
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East Asian
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DP
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ClippingRankSum
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QD
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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VQSLOD
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FS
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SIO_000300: 9.66e-1

MQ
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SIO_000300: 5.913e1

ReadPosRankSum
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SIO_000300: 7.13e-1

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

European (Non-Finnish)
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East Asian
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South Asian
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Latino
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Other
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MQRankSum
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QD
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InbreedingCoeff
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BaseQRankSum
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MQ
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FS
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DP
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ClippingRankSum
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VQSLOD
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SIO_000300: 1.79e0

ReadPosRankSum
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SIO_000300: 3.92e-1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
type: Population
allele count: 481
allele frequency: 7.274652147610405e-2
allele num: 6612
num of homozygotes: 17

African
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allele count: 139
allele frequency: 1.336795537603385e-2
allele num: 10398
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European (Non-Finnish)
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allele count: 5224
allele frequency: 7.834433113377325e-2
allele num: 66680
num of homozygotes: 183

Latino
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allele count: 517
allele frequency: 4.467680608365019e-2
allele num: 11572
num of homozygotes: 13

South Asian
type: Population
allele count: 2807
allele frequency: 1.700593723494487e-1
allele num: 16506
num of homozygotes: 266

East Asian
type: Population
allele count: 289
allele frequency: 3.341040462427745e-2
allele num: 8650
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Other
type: Population
allele count: 76
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allele num: 906
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InbreedingCoeff
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MQRankSum
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MQ
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SIO_000300: 5.93e1

BaseQRankSum
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ReadPosRankSum
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SIO_000300: 5.81e-1

FS
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VQSLOD
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ClippingRankSum
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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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GenotypeQuality
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GenotypeQuality
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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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Latino
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Other
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African
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South Asian
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European (Non-Finnish)
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ReadPosRankSum
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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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VQSLOD
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ClippingRankSum
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MQ
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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East Asian
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Other
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South Asian
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European (Non-Finnish)
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InbreedingCoeff
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MQ
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DP
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QD
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VQSLOD
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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FS
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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East Asian
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African
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European (Non-Finnish)
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European (Finnish)
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South Asian
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VQSLOD
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MQRankSum
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FS
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InbreedingCoeff
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MQ
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BaseQRankSum
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ReadPosRankSum
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QD
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DP
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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East Asian
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African
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Latino
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European (Finnish)
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Other
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BaseQRankSum
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InbreedingCoeff
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MQ
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ReadPosRankSum
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DP
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VQSLOD
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FS
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MQRankSum
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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South Asian
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Other
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African
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European (Finnish)
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East Asian
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Latino
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VQSLOD
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FS
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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DP
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MQ
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QD
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ReadPosRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 6

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allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

European (Finnish)
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allele count: 29
allele frequency: 4.656390494540783e-3
allele num: 6228
num of homozygotes: 0

Other
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allele frequency: 1.11358574610245e-3
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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

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

European (Non-Finnish)
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allele count: 4
allele frequency: 6.003301815998799e-5
allele num: 66630
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

ClippingRankSum
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FS
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VQSLOD
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MQ
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ReadPosRankSum
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DP
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BaseQRankSum
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MQRankSum
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SIO_000300: 1.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

QD
type: SiteQuality
SIO_000300: 3.1e-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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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5365
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498845888665727e-5
allele num: 66718
num of homozygotes: 0

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

East Asian
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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

DP
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SIO_000300: 1.978589e6

MQ
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SIO_000300: 5.985e1

FS
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SIO_000300: 5.829e0

ReadPosRankSum
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QD
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BaseQRankSum
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ClippingRankSum
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SIO_000300: -8.98e-1

MQRankSum
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SIO_000300: 1.72e0

VQSLOD
type: SiteQuality
SIO_000300: -1.115e-1

InbreedingCoeff
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SIO_000300: 0.0e0

GenotypeDepth
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bin: 7.5e0
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: 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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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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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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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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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: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

Other
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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: 8654
num of homozygotes: 0

South Asian
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allele count: 1
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allele num: 16512
num of homozygotes: 0

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

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

InbreedingCoeff
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SIO_000300: 0.0e0

ReadPosRankSum
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SIO_000300: 1.14e0

QD
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SIO_000300: 1.223e1

DP
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SIO_000300: 1.978502e6

ClippingRankSum
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BaseQRankSum
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VQSLOD
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SIO_000300: 6.919999999999999e-1

MQRankSum
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SIO_000300: -3.08e-1

FS
type: SiteQuality
SIO_000300: 3.765e0

MQ
type: SiteQuality
SIO_000300: 5.944e1

GenotypeDepth
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bin: 9.25e1
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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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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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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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele num: 16512
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
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MQRankSum
type: SiteQuality
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VQSLOD
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MQ
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InbreedingCoeff
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FS
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ClippingRankSum
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QD
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DP
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BaseQRankSum
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ReadPosRankSum
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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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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 0.0e0
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Latino
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South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 1.51285930408472e-4
allele num: 6610
num of homozygotes: 0

African
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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QD
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VQSLOD
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DP
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MQRankSum
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FS
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BaseQRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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Latino
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African
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South Asian
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European (Finnish)
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Other
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BaseQRankSum
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QD
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MQ
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FS
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MQRankSum
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 66712
num of homozygotes: 0

African
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num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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Other
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Latino
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African
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East Asian
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allele num: 8638
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South Asian
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MQ
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ReadPosRankSum
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MQRankSum
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FS
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ClippingRankSum
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BaseQRankSum
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DP
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QD
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InbreedingCoeff
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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Latino
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European (Non-Finnish)
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European (Finnish)
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African
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South Asian
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DP
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MQRankSum
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MQ
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FS
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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QD
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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European (Finnish)
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Other
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African
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European (Non-Finnish)
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Latino
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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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BaseQRankSum
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DP
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VQSLOD
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ClippingRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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Latino
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European (Non-Finnish)
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African
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Other
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MQ
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ReadPosRankSum
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VQSLOD
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DP
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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FS
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 1.506160195198361e-5
allele num: 66394
num of homozygotes: 0

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

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South Asian
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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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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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FS
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MQ
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QD
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VQSLOD
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InbreedingCoeff
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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Latino
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Other
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European (Finnish)
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South Asian
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European (Non-Finnish)
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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MQ
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InbreedingCoeff
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MQRankSum
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DP
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FS
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BaseQRankSum
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QD
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GenotypeDepth
all individuals: 252
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
all individuals: 465
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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
all individuals: 20
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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