1-25712334-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25712334
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25712334
    reference: chr 1
allele count: 233
allele frequency: 1.919085428129015e-3
allele num: 121412
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.626T>C
  hgvsp: ENSP00000345084.4:p.Val209Ala
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.626T>C
  hgvsp: ENSP00000416275.1:p.Val209Ala
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.941T>C
  hgvsp: ENSP00000415417.1:p.Val314Ala
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.893T>C
  hgvsp: ENSP00000363472.2:p.Val298Ala
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.488T>C
  hgvsp: ENSP00000344485.4:p.Val163Ala
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.1096T>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+4906T>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.939+3133T>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*271T>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.893T>C
  hgvsp: ENSP00000311185.4:p.Val298Ala
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.941T>C
  hgvsp: ENSP00000294413.6:p.Val314Ala
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.941T>C
  hgvsp: ENSP00000243186.6:p.Val314Ala
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.108-10415T>C
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4625
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3513
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20099
  bin: 9.75e1
  variant carriers: 198
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4658
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2877
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Val314Ala
num of homozygotes: 1
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

1-25712353-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25712353
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25712353
    reference: chr 1
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.940-18A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.940-18A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-18A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.1095-18A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.625-18A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+4887A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.892-18A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*270-18A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.940-18A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.892-18A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.939+3114A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.625-18A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.108-10434A>G
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4592
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4668
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4898
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4631
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3533
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19978
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1723
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

1-25712358-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25712358
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25712358
    reference: chr 1
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.892-23C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.108-10439C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.625-23C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.940-23C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+4882C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.940-23C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.892-23C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*270-23C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-23C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.1095-23C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.625-23C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.939+3109C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.940-23C>T
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4592
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3533
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4143
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1723
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4898
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19978
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

1-25712363-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25712363
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25712363
    reference: chr 1
allele count: 3
allele frequency: 2.471006852925672e-5
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.892-28A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.939+3104A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-28A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.625-28A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*270-28A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.940-28A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.892-28A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.1095-28A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+4877A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.940-28A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.940-28A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.108-10444A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.625-28A>G
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3532
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19978
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4142
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4631
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4592
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1723
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4668
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4164
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD

1-25712367-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25712367
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25712367
    reference: chr 1
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.940-32G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+4873G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.939+3100G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.940-32G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.892-32G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*270-32G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.1095-32G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.625-32G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.108-10448G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.940-32G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.625-32G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.892-32G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-32G>C
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4592
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4142
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4669
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4631
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1723
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3533
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4898
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2230
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

1-25712369-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25712369
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25712369
    reference: chr 1
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+4871C>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.940-34C>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.625-34C>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.939+3098C>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.625-34C>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.940-34C>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.108-10450C>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.940-34C>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.892-34C>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.1095-34C>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.892-34C>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*270-34C>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-34C>G
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4592
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19976
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2891
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4670
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4898
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3534
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-25712370-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25712370
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25712370
    reference: chr 1
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.625-35C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.892-35C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+4870C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.625-35C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.108-10451C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.1095-35C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-35C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.892-35C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*270-35C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.940-35C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.940-35C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.939+3097C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.940-35C>T
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4631
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2891
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2231
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4164
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4898
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1721
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4670
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4142
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: African
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

1-25715426-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715426
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715426
    reference: chr 1
allele count: 1
allele frequency: 8.253412786187088e-6
allele num: 121162
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*269+41G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.624+41G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1814G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.891+41G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.624+41G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.1094+41G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.891+41G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.939+41G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.939+41G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3091G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.108-13507G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.939+41G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.939+41G>A
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9655
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2278
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12194
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25941
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

1-25715432-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715432
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715432
    reference: chr 1
allele count: 38
allele frequency: 3.135313531353136e-4
allele num: 121200
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.939+35G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.624+35G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*269+35G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.891+35G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.891+35G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.939+35G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.1094+35G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.939+35G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.624+35G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1808G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.939+35G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3097G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.108-13513G>A
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2278
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26118
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 12518
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9690
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

1-25715444-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715444
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715444
    reference: chr 1
allele count: 2
allele frequency: 1.64923970049807e-5
allele num: 121268
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.891+23C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.891+23C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3109C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.939+23C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.624+23C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.1094+23C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.939+23C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.108-13525C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1796C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.939+23C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.939+23C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.624+23C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*269+23C>T
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26406
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12670
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2269
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9715
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum

1-25715453-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715453
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715453
    reference: chr 1
allele count: 1
allele frequency: 8.243751236562685e-6
allele num: 121304
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.108-13534C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*269+14C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.624+14C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1787C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.939+14C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.624+14C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.891+14C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.939+14C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.1094+14C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.891+14C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.939+14C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.939+14C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3118C>T
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12682
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26494
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9729
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2269
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD

1-25715463-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715463
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715463
    reference: chr 1
allele count: 1
allele frequency: 8.241848811525402e-6
allele num: 121332
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.624+4A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.624+4A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.939+4A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*269+4A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3128A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.939+4A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.1094+4A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1777A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.939+4A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.891+4A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.108-13544A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.891+4A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.939+4A>G
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2277
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12661
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26525
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9747
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.939+4A>G
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

http://identifiers.org/exac.variant/1-25715466-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715466
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715466
    reference: chr 1
allele count: 2
allele frequency: 1.648750247312537e-5
allele num: 121304
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.891+1G>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*269+1G>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.939+1G>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.108-13547G>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.624+1G>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.939+1G>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.1094+1G>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1774G>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.624+1G>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3131G>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.891+1G>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.939+1G>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.939+1G>T
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: splice donor
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9758
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12443
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26425
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.939+1G>T
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

1-25715467-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715467
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715467
    reference: chr 1
allele count: 2
allele frequency: 1.648559982854976e-5
allele num: 121318
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.1094G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1773G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.939G>A
  hgvsp: ENST00000413854.1:c.939G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.108-13548G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.624G>A
  hgvsp: ENST00000455194.1:c.624G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.939G>A
  hgvsp: ENST00000243186.6:c.939G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.891G>A
  hgvsp: ENST00000374352.2:c.891G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*269G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.624G>A
  hgvsp: ENST00000340849.4:c.624G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.939G>A
  hgvsp: ENST00000349438.4:c.939G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.939G>A
  hgvsp: ENST00000294413.7:c.939G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3132G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.891G>A
  hgvsp: ENST00000349320.3:c.891G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1358
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9761
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.939G>A
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP

1-25715468-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715468
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715468
    reference: chr 1
allele count: 5
allele frequency: 4.120992334954257e-5
allele num: 121330
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.938C>T
  hgvsp: ENSP00000243186.6:p.Pro313Leu
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.938C>T
  hgvsp: ENSP00000334570.5:p.Pro313Leu
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.890C>T
  hgvsp: ENSP00000311185.4:p.Pro297Leu
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.938C>T
  hgvsp: ENSP00000415417.1:p.Pro313Leu
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.890C>T
  hgvsp: ENSP00000363472.2:p.Pro297Leu
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1772C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.938C>T
  hgvsp: ENSP00000294413.6:p.Pro313Leu
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.623C>T
  hgvsp: ENSP00000416275.1:p.Pro208Leu
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*268C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.108-13549C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.623C>T
  hgvsp: ENSP00000345084.4:p.Pro208Leu
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.1093C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3133C>T
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9771
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26490
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro313Leu
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum

1-25715474-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715474
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715474
    reference: chr 1
allele count: 3
allele frequency: 2.474430880897394e-5
allele num: 121240
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.617G>A
  hgvsp: ENSP00000345084.4:p.Cys206Tyr
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*262G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3139G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.617G>A
  hgvsp: ENSP00000416275.1:p.Cys206Tyr
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.108-13555G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.884G>A
  hgvsp: ENSP00000311185.4:p.Cys295Tyr
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.1087G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.932G>A
  hgvsp: ENSP00000415417.1:p.Cys311Tyr
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.932G>A
  hgvsp: ENSP00000243186.6:p.Cys311Tyr
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.932G>A
  hgvsp: ENSP00000334570.5:p.Cys311Tyr
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.884G>A
  hgvsp: ENSP00000363472.2:p.Cys295Tyr
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1766G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.932G>A
  hgvsp: ENSP00000294413.6:p.Cys311Tyr
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2252
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12446
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26577
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys311Tyr
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

1-25715476-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715476
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715476
    reference: chr 1
allele count: 1
allele frequency: 8.241441263248117e-6
allele num: 121338
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.930G>A
  hgvsp: ENST00000294413.7:c.930G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*260G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.882G>A
  hgvsp: ENST00000349320.3:c.882G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.930G>A
  hgvsp: ENST00000413854.1:c.930G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.615G>A
  hgvsp: ENST00000340849.4:c.615G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3141G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.882G>A
  hgvsp: ENST00000374352.2:c.882G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.930G>A
  hgvsp: ENST00000349438.4:c.930G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1764G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.615G>A
  hgvsp: ENST00000455194.1:c.615G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.108-13557G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.1085G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.930G>A
  hgvsp: ENST00000243186.6:c.930G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9780
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26588
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12409
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys310Lys
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

1-25715487-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715487
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715487
    reference: chr 1
allele count: 1
allele frequency: 8.243751236562685e-6
allele num: 121304
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.604G>C
  hgvsp: ENSP00000416275.1:p.Gly202Arg
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.919G>C
  hgvsp: ENSP00000243186.6:p.Gly307Arg
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3152G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1753G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.871G>C
  hgvsp: ENSP00000363472.2:p.Gly291Arg
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.108-13568G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.1074G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.604G>C
  hgvsp: ENSP00000345084.4:p.Gly202Arg
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*249G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.871G>C
  hgvsp: ENSP00000311185.4:p.Gly291Arg
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.919G>C
  hgvsp: ENSP00000415417.1:p.Gly307Arg
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.919G>C
  hgvsp: ENSP00000294413.6:p.Gly307Arg
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.919G>C
  hgvsp: ENSP00000334570.5:p.Gly307Arg
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26558
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12303
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9793
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly307Arg
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

1-25715487-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715487
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715487
    reference: chr 1
allele count: 11
allele frequency: 9.068126360218954e-5
allele num: 121304
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.871G>A
  hgvsp: ENSP00000363472.2:p.Gly291Arg
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.108-13568G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.604G>A
  hgvsp: ENSP00000416275.1:p.Gly202Arg
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.919G>A
  hgvsp: ENSP00000334570.5:p.Gly307Arg
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3152G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*249G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.919G>A
  hgvsp: ENSP00000415417.1:p.Gly307Arg
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.871G>A
  hgvsp: ENSP00000311185.4:p.Gly291Arg
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.604G>A
  hgvsp: ENSP00000345084.4:p.Gly202Arg
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.919G>A
  hgvsp: ENSP00000243186.6:p.Gly307Arg
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.919G>A
  hgvsp: ENSP00000294413.6:p.Gly307Arg
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.1074G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1753G>A
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12303
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9793
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26558
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gly307Arg
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP

1-25715488-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715488
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715488
    reference: chr 1
allele count: 1
allele frequency: 8.246606521416436e-6
allele num: 121262
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.918C>T
  hgvsp: ENST00000294413.7:c.918C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.918C>T
  hgvsp: ENST00000349438.4:c.918C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*248C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.918C>T
  hgvsp: ENST00000243186.6:c.918C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.870C>T
  hgvsp: ENST00000349320.3:c.870C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.603C>T
  hgvsp: ENST00000340849.4:c.603C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.603C>T
  hgvsp: ENST00000455194.1:c.603C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.918C>T
  hgvsp: ENST00000413854.1:c.918C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3153C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.1073C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.870C>T
  hgvsp: ENST00000374352.2:c.870C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1752C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.108-13569C>T
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12331
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile306Ile
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

1-25715488-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715488
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715488
    reference: chr 1
allele count: 1
allele frequency: 8.246606521416436e-6
allele num: 121262
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.918C>A
  hgvsp: ENST00000243186.6:c.918C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.108-13569C>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.603C>A
  hgvsp: ENST00000340849.4:c.603C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.918C>A
  hgvsp: ENST00000294413.7:c.918C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.1073C>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.870C>A
  hgvsp: ENST00000374352.2:c.870C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.870C>A
  hgvsp: ENST00000349320.3:c.870C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3153C>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.918C>A
  hgvsp: ENST00000413854.1:c.918C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.603C>A
  hgvsp: ENST00000455194.1:c.603C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.918C>A
  hgvsp: ENST00000349438.4:c.918C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1752C>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*248C>A
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9799
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12331
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile306Ile
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

1-25715490-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715490
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715490
    reference: chr 1
allele count: 62
allele frequency: 5.115511551155115e-4
allele num: 121200
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.868A>G
  hgvsp: ENSP00000311185.4:p.Ile290Val
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.108-13571A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.916A>G
  hgvsp: ENSP00000334570.5:p.Ile306Val
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*246A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.868A>G
  hgvsp: ENSP00000363472.2:p.Ile290Val
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.916A>G
  hgvsp: ENSP00000294413.6:p.Ile306Val
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.916A>G
  hgvsp: ENSP00000415417.1:p.Ile306Val
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.601A>G
  hgvsp: ENSP00000416275.1:p.Ile201Val
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.601A>G
  hgvsp: ENSP00000345084.4:p.Ile201Val
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.1071A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1750A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3155A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.916A>G
  hgvsp: ENSP00000243186.6:p.Ile306Val
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 4.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 12317
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Ile306Val
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQ

1-25715494-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715494
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715494
    reference: chr 1
allele count: 1
allele frequency: 8.244974687927709e-6
allele num: 121286
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.864C>G
  hgvsp: ENSP00000363472.2:p.Ile288Met
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.912C>G
  hgvsp: ENSP00000415417.1:p.Ile304Met
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.864C>G
  hgvsp: ENSP00000311185.4:p.Ile288Met
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.912C>G
  hgvsp: ENSP00000294413.6:p.Ile304Met
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1746C>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.108-13575C>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.597C>G
  hgvsp: ENSP00000416275.1:p.Ile199Met
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.912C>G
  hgvsp: ENSP00000243186.6:p.Ile304Met
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*242C>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.912C>G
  hgvsp: ENSP00000334570.5:p.Ile304Met
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3159C>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.597C>G
  hgvsp: ENSP00000345084.4:p.Ile199Met
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.1067C>G
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26587
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2267
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9806
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12345
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile304Met
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum

1-25715497-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715497
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715497
    reference: chr 1
allele count: 1
allele frequency: 8.244294947896055e-6
allele num: 121296
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.909G>C
  hgvsp: ENST00000349438.4:c.909G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.861G>C
  hgvsp: ENST00000374352.2:c.861G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.909G>C
  hgvsp: ENST00000413854.1:c.909G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.909G>C
  hgvsp: ENST00000294413.7:c.909G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.1064G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.594G>C
  hgvsp: ENST00000455194.1:c.594G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1743G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.861G>C
  hgvsp: ENST00000349320.3:c.861G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*239G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.909G>C
  hgvsp: ENST00000243186.6:c.909G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3162G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.594G>C
  hgvsp: ENST00000340849.4:c.594G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.108-13578G>C
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12325
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu303Leu
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-25715498-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715498
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715497
    reference: chr 1
allele count: 2
allele frequency: 1.650410126916539e-5
allele num: 121182
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.592delC
  hgvsp: ENSP00000416275.1:p.Leu198Ter
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.859delC
  hgvsp: ENSP00000363472.2:p.Leu287Ter
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.907delC
  hgvsp: ENSP00000294413.6:p.Leu303Ter
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*237delC
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.859delC
  hgvsp: ENSP00000311185.4:p.Leu287Ter
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.108-13580delC
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.907delC
  hgvsp: ENSP00000334570.5:p.Leu303Ter
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.907delC
  hgvsp: ENSP00000243186.6:p.Leu303Ter
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1741delC
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.592delC
  hgvsp: ENSP00000345084.4:p.Leu198Ter
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3164delC
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.907delC
  hgvsp: ENSP00000415417.1:p.Leu303Ter
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.1062delC
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12310
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26594
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu303Ter
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: AG
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

1-25715499-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715499
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715499
    reference: chr 1
allele count: 13
allele frequency: 1.104671912442005e-4
allele num: 117682
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*237C>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.907C>G
  hgvsp: ENSP00000334570.5:p.Leu303Val
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.592C>G
  hgvsp: ENSP00000345084.4:p.Leu198Val
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1741C>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3164C>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.907C>G
  hgvsp: ENSP00000243186.6:p.Leu303Val
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.859C>G
  hgvsp: ENSP00000363472.2:p.Leu287Val
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.907C>G
  hgvsp: ENSP00000415417.1:p.Leu303Val
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.592C>G
  hgvsp: ENSP00000416275.1:p.Leu198Val
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.1062C>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.859C>G
  hgvsp: ENSP00000311185.4:p.Leu287Val
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.108-13580C>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.907C>G
  hgvsp: ENSP00000294413.6:p.Leu303Val
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9675
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2279
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12057
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu303Val
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

1-25715505-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715505
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715505
    reference: chr 1
allele count: 1
allele frequency: 8.241441263248117e-6
allele num: 121338
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.901G>A
  hgvsp: ENSP00000415417.1:p.Ala301Thr
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.853G>A
  hgvsp: ENSP00000311185.4:p.Ala285Thr
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.901G>A
  hgvsp: ENSP00000334570.5:p.Ala301Thr
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.901G>A
  hgvsp: ENSP00000294413.6:p.Ala301Thr
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.586G>A
  hgvsp: ENSP00000345084.4:p.Ala196Thr
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.853G>A
  hgvsp: ENSP00000363472.2:p.Ala285Thr
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+13582G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.586G>A
  hgvsp: ENSP00000416275.1:p.Ala196Thr
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*231G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.901G>A
  hgvsp: ENSP00000243186.6:p.Ala301Thr
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1735G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.1056G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3170G>A
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10170
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12179
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27037
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala301Thr
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

http://identifiers.org/exac.variant/1-25715515-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715515
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715515
    reference: chr 1
allele count: 2
allele frequency: 1.648587160803192e-5
allele num: 121316
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.891G>T
  hgvsp: ENST00000413854.1:c.891G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.891G>T
  hgvsp: ENST00000243186.6:c.891G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3180G>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.891G>T
  hgvsp: ENST00000294413.7:c.891G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.843G>T
  hgvsp: ENST00000349320.3:c.843G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.843G>T
  hgvsp: ENST00000374352.2:c.843G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.891G>T
  hgvsp: ENST00000349438.4:c.891G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.576G>T
  hgvsp: ENST00000340849.4:c.576G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1725G>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.1046G>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.576G>T
  hgvsp: ENST00000455194.1:c.576G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*221G>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+13572G>T
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10156
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2412
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12151
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27022
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu297Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

1-25715516-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715516
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715516
    reference: chr 1
allele count: 4
allele frequency: 3.297065611605671e-5
allele num: 121320
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.842T>C
  hgvsp: ENSP00000311185.4:p.Leu281Pro
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.890T>C
  hgvsp: ENSP00000294413.6:p.Leu297Pro
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.575T>C
  hgvsp: ENSP00000345084.4:p.Leu192Pro
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.890T>C
  hgvsp: ENSP00000243186.6:p.Leu297Pro
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.575T>C
  hgvsp: ENSP00000416275.1:p.Leu192Pro
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3181T>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+13571T>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*220T>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.1045T>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.890T>C
  hgvsp: ENSP00000334570.5:p.Leu297Pro
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.842T>C
  hgvsp: ENSP00000363472.2:p.Leu281Pro
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1724T>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.890T>C
  hgvsp: ENSP00000415417.1:p.Leu297Pro
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12146
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27024
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu297Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

1-25715520-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715520
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715520
    reference: chr 1
allele count: 1
allele frequency: 8.243887157672586e-6
allele num: 121302
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.886G>A
  hgvsp: ENSP00000243186.6:p.Val296Met
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.886G>A
  hgvsp: ENSP00000334570.5:p.Val296Met
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+13567G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.838G>A
  hgvsp: ENSP00000363472.2:p.Val280Met
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*216G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.1041G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.838G>A
  hgvsp: ENSP00000311185.4:p.Val280Met
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.571G>A
  hgvsp: ENSP00000416275.1:p.Val191Met
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.571G>A
  hgvsp: ENSP00000345084.4:p.Val191Met
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3185G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.886G>A
  hgvsp: ENSP00000294413.6:p.Val296Met
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.886G>A
  hgvsp: ENSP00000415417.1:p.Val296Met
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1720G>A
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12105
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10141
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val296Met
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP

1-25715526-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715526
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715526
    reference: chr 1
allele count: 1
allele frequency: 8.24783082049421e-6
allele num: 121244
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.565G>A
  hgvsp: ENSP00000345084.4:p.Ala189Thr
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.880G>A
  hgvsp: ENSP00000294413.6:p.Ala294Thr
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*210G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.832G>A
  hgvsp: ENSP00000363472.2:p.Ala278Thr
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3191G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.880G>A
  hgvsp: ENSP00000334570.5:p.Ala294Thr
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.832G>A
  hgvsp: ENSP00000311185.4:p.Ala278Thr
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.880G>A
  hgvsp: ENSP00000415417.1:p.Ala294Thr
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.1035G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1714G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+13561G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.565G>A
  hgvsp: ENSP00000416275.1:p.Ala189Thr
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.880G>A
  hgvsp: ENSP00000243186.6:p.Ala294Thr
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12074
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10133
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala294Thr
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD

1-25715533-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715533
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715533
    reference: chr 1
allele count: 22
allele frequency: 1.814522780508726e-4
allele num: 121244
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.873G>A
  hgvsp: ENST00000294413.7:c.873G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.558G>A
  hgvsp: ENST00000340849.4:c.558G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.825G>A
  hgvsp: ENST00000349320.3:c.825G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.873G>A
  hgvsp: ENST00000243186.6:c.873G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.873G>A
  hgvsp: ENST00000413854.1:c.873G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3198G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.1028G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1707G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*203G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.558G>A
  hgvsp: ENST00000455194.1:c.558G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.825G>A
  hgvsp: ENST00000374352.2:c.825G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+13554G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.873G>A
  hgvsp: ENST00000349438.4:c.873G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 11976
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26999
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro291Pro
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

1-25715534-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715534
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715534
    reference: chr 1
allele count: 8
allele frequency: 6.59870005608895e-5
allele num: 121236
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3199C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.872C>T
  hgvsp: ENSP00000415417.1:p.Pro291Leu
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.557C>T
  hgvsp: ENSP00000345084.4:p.Pro186Leu
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.557C>T
  hgvsp: ENSP00000416275.1:p.Pro186Leu
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.872C>T
  hgvsp: ENSP00000294413.6:p.Pro291Leu
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.824C>T
  hgvsp: ENSP00000311185.4:p.Pro275Leu
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.1027C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.824C>T
  hgvsp: ENSP00000363472.2:p.Pro275Leu
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1706C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*202C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+13553C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.872C>T
  hgvsp: ENSP00000334570.5:p.Pro291Leu
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.872C>T
  hgvsp: ENSP00000243186.6:p.Pro291Leu
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26998
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2404
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10115
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11965
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro291Leu
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

1-25715548-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715548
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715548
    reference: chr 1
allele count: 1
allele frequency: 8.269520202437855e-6
allele num: 120926
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.858C>A
  hgvsp: ENSP00000243186.6:p.His286Gln
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.858C>A
  hgvsp: ENSP00000415417.1:p.His286Gln
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.1013C>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.543C>A
  hgvsp: ENSP00000416275.1:p.His181Gln
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.858C>A
  hgvsp: ENSP00000294413.6:p.His286Gln
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.810C>A
  hgvsp: ENSP00000363472.2:p.His270Gln
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.810C>A
  hgvsp: ENSP00000311185.4:p.His270Gln
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.543C>A
  hgvsp: ENSP00000345084.4:p.His181Gln
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.858C>A
  hgvsp: ENSP00000334570.5:p.His286Gln
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3213C>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1692C>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+13539C>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*188C>A
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 26611
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11957
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9803
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His286Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

1-25715554-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715554
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715554
    reference: chr 1
allele count: 35
allele frequency: 2.902252147666589e-4
allele num: 120596
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.852G>A
  hgvsp: ENST00000294413.7:c.852G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.537G>A
  hgvsp: ENST00000340849.4:c.537G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.1007G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.852G>A
  hgvsp: ENST00000413854.1:c.852G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.804G>A
  hgvsp: ENST00000374352.2:c.804G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*182G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.537G>A
  hgvsp: ENST00000455194.1:c.537G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.852G>A
  hgvsp: ENST00000243186.6:c.852G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.804G>A
  hgvsp: ENST00000349320.3:c.804G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1686G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.852G>A
  hgvsp: ENST00000349438.4:c.852G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3219G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+13533G>A
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2143
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12085
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9672
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser284Ser
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ

1-25715557-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715557
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715557
    reference: chr 1
allele count: 2
allele frequency: 1.661488361274029e-5
allele num: 120374
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.849C>G
  hgvsp: ENST00000413854.1:c.849C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.1004C>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.801C>G
  hgvsp: ENST00000349320.3:c.801C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.801C>G
  hgvsp: ENST00000374352.2:c.801C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3222C>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*179C>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.849C>G
  hgvsp: ENST00000243186.6:c.849C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.849C>G
  hgvsp: ENST00000294413.7:c.849C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+13530C>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.534C>G
  hgvsp: ENST00000455194.1:c.534C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.534C>G
  hgvsp: ENST00000340849.4:c.534C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1683C>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.849C>G
  hgvsp: ENST00000349438.4:c.849C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12075
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26820
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9700
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2104
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr283Thr
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

1-25715571-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715571
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715571
    reference: chr 1
allele count: 1
allele frequency: 8.285827919925758e-6
allele num: 120688
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.520G>A
  hgvsp: ENSP00000416275.1:p.Val174Met
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.835G>A
  hgvsp: ENSP00000415417.1:p.Val279Met
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3236G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+13516G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.520G>A
  hgvsp: ENSP00000345084.4:p.Val174Met
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.835G>A
  hgvsp: ENSP00000294413.6:p.Val279Met
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.835G>A
  hgvsp: ENSP00000243186.6:p.Val279Met
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1669G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.835G>A
  hgvsp: ENSP00000334570.5:p.Val279Met
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.787G>A
  hgvsp: ENSP00000311185.4:p.Val263Met
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.787G>A
  hgvsp: ENSP00000363472.2:p.Val263Met
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.990G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*165G>A
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12339
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27241
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val279Met
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

1-25715572-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715572
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715572
    reference: chr 1
allele count: 2
allele frequency: 1.657357840131263e-5
allele num: 120674
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.834C>T
  hgvsp: ENST00000294413.7:c.834C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.519C>T
  hgvsp: ENST00000340849.4:c.519C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+13515C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.834C>T
  hgvsp: ENST00000349438.4:c.834C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.519C>T
  hgvsp: ENST00000455194.1:c.519C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.786C>T
  hgvsp: ENST00000349320.3:c.786C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1668C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.989C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3237C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.786C>T
  hgvsp: ENST00000374352.2:c.786C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*164C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.834C>T
  hgvsp: ENST00000243186.6:c.834C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.834C>T
  hgvsp: ENST00000413854.1:c.834C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9698
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27260
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12352
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly278Gly
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: DP

1-25715587-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715587
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715587
    reference: chr 1
allele count: 2
allele frequency: 1.662869780667476e-5
allele num: 120274
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.819G>A
  hgvsp: ENST00000413854.1:c.819G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.819G>A
  hgvsp: ENST00000349438.4:c.819G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.819G>A
  hgvsp: ENST00000294413.7:c.819G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.504G>A
  hgvsp: ENST00000340849.4:c.504G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+13500G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.771G>A
  hgvsp: ENST00000374352.2:c.771G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.771G>A
  hgvsp: ENST00000349320.3:c.771G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.819G>A
  hgvsp: ENST00000243186.6:c.819G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.974G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.504G>A
  hgvsp: ENST00000455194.1:c.504G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*149G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3252G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1653G>A
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27298
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1974
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12163
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala273Ala
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

1-25715588-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715588
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715588
    reference: chr 1
allele count: 36
allele frequency: 2.997002997002997e-4
allele num: 120120
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.503C>T
  hgvsp: ENSP00000416275.1:p.Ala168Val
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3253C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.818C>T
  hgvsp: ENSP00000415417.1:p.Ala273Val
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.503C>T
  hgvsp: ENSP00000345084.4:p.Ala168Val
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.770C>T
  hgvsp: ENSP00000363472.2:p.Ala257Val
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.973C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.770C>T
  hgvsp: ENSP00000311185.4:p.Ala257Val
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+13499C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.818C>T
  hgvsp: ENSP00000294413.6:p.Ala273Val
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.818C>T
  hgvsp: ENSP00000334570.5:p.Ala273Val
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1652C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.818C>T
  hgvsp: ENSP00000243186.6:p.Ala273Val
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*148C>T
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9613
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27252
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 4.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12066
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala273Val
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD

1-25715596-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715596
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715596
    reference: chr 1
allele count: 2
allele frequency: 1.672268767036238e-5
allele num: 119598
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.762G>A
  hgvsp: ENST00000374352.2:c.762G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.810G>A
  hgvsp: ENST00000349438.4:c.810G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.495G>A
  hgvsp: ENST00000455194.1:c.495G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+13491G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.810G>A
  hgvsp: ENST00000243186.6:c.810G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.810G>A
  hgvsp: ENST00000413854.1:c.810G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.810G>A
  hgvsp: ENST00000294413.7:c.810G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3261G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1644G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.495G>A
  hgvsp: ENST00000340849.4:c.495G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.762G>A
  hgvsp: ENST00000349320.3:c.762G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*140G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.965G>A
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11726
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27089
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val270Val
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/1-25715599-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715599
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715599
    reference: chr 1
allele count: 2
allele frequency: 1.679966400671986e-5
allele num: 119050
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.759T>G
  hgvsp: ENSP00000363472.2:p.Tyr253Ter
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.962T>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.492T>G
  hgvsp: ENSP00000416275.1:p.Tyr164Ter
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.807T>G
  hgvsp: ENSP00000243186.6:p.Tyr269Ter
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*137T>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.807T>G
  hgvsp: ENSP00000334570.5:p.Tyr269Ter
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.759T>G
  hgvsp: ENSP00000311185.4:p.Tyr253Ter
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.807T>G
  hgvsp: ENSP00000294413.6:p.Tyr269Ter
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3264T>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.492T>G
  hgvsp: ENSP00000345084.4:p.Tyr164Ter
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+13488T>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1641T>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.807T>G
  hgvsp: ENSP00000415417.1:p.Tyr269Ter
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: stop gained
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11403
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9341
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26822
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr269Ter
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD

1-25715600-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715600
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715600
    reference: chr 1
allele count: 10
allele frequency: 8.396446623788812e-5
allele num: 119098
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.806A>G
  hgvsp: ENSP00000243186.6:p.Tyr269Cys
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.491A>G
  hgvsp: ENSP00000416275.1:p.Tyr164Cys
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3265A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1640A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.806A>G
  hgvsp: ENSP00000415417.1:p.Tyr269Cys
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.758A>G
  hgvsp: ENSP00000311185.4:p.Tyr253Cys
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.806A>G
  hgvsp: ENSP00000334570.5:p.Tyr269Cys
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.491A>G
  hgvsp: ENSP00000345084.4:p.Tyr164Cys
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.806A>G
  hgvsp: ENSP00000294413.6:p.Tyr269Cys
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.758A>G
  hgvsp: ENSP00000363472.2:p.Tyr253Cys
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.961A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*136A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+13487A>G
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11429
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26848
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9334
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr269Cys
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD

1-25715619-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715619
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715619
    reference: chr 1
allele count: 1
allele frequency: 8.701705534284719e-6
allele num: 114920
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.802-15G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1621G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3284G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.487-15G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.487-15G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.802-15G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.754-15G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.802-15G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.802-15G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*132-15G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.957-15G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.754-15G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+13468G>A
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9104
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2903
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22714
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6612
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8012
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: African
reference allele: C
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

1-25715620-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715620
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715620
    reference: chr 1
allele count: 59
allele frequency: 5.142329213659421e-4
allele num: 114734
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.802-16C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.754-16C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3285C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.802-16C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.754-16C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.957-16C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.802-16C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.487-16C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1620C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.802-16C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.487-16C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+13467C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*132-16C>T
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8958
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3006
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7816
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7089
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22394
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1725
  bin: 3.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: Latino
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP

1-25715626-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715626
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715626
    reference: chr 1
allele count: 1
allele frequency: 8.849087659062351e-6
allele num: 113006
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.754-22C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3291C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.802-22C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.487-22C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+13461C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.487-22C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.802-22C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.802-22C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.957-22C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.754-22C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1614C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.802-22C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*132-22C>T
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10827
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2336
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3633
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7593
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6880
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19214
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/1-25715642-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715642
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715642
    reference: chr 1
allele count: 1
allele frequency: 9.22509225092251e-6
allele num: 108400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.487-38T>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.957-38T>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.802-38T>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.487-38T>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3307T>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.802-38T>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1598T>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.802-38T>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+13445T>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*132-38T>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.754-38T>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.754-38T>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.802-38T>G
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8362
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16639
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12121
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2981
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

1-25715645-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715645
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715645
    reference: chr 1
allele count: 2
allele frequency: 1.867727535907062e-5
allele num: 107082
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+13442C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.802-41C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1595C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.802-41C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3310C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.487-41C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.754-41C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.754-41C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.802-41C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.957-41C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.487-41C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.802-41C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*132-41C>T
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2669
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13892
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16264
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5563
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4774
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6779
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

1-25715649-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25715649
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25715649
    reference: chr 1
allele count: 13
allele frequency: 1.233302975106254e-4
allele num: 105408
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.754-45C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.802-45C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.754-45C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.487-45C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.802-45C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.957-45C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.487-45C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.802-45C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.802-45C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+13438C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-3314C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+1591C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*132-45C>T
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6348
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5046
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6340
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14092
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD

1-25717191-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25717191
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25717191
    reference: chr 1
allele count: 1
allele frequency: 8.244566830458728e-6
allele num: 121292
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.956+49C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+11896C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.801+49C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.753+49C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.487-1587C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-4856C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.801+49C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.753+49C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.801+49C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.487-1587C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+49C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.801+49C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*132-1587C>T
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7660
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5846
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2070
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2759
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7395
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7128
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6072
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4320
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4697
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3780
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2531
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

1-25717193-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25717193
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25717193
    reference: chr 1
allele count: 3
allele frequency: 2.473084595980413e-5
allele num: 121306
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.487-1589A>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.956+47A>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.801+47A>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.801+47A>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.753+47A>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+11894A>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.753+47A>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-4858A>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.801+47A>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+47A>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.801+47A>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*132-1589A>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.487-1589A>C
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7396
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3780
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2758
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2071
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5846
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4697
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6077
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2520
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4341
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

1-25717206-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25717206
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25717206
    reference: chr 1
allele count: 1
allele frequency: 8.244702778464837e-6
allele num: 121290
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.801+34G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+11881G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.753+34G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.487-1602G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*132-1602G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.801+34G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.753+34G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.487-1602G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.801+34G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.956+34G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.801+34G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-4871G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+34G>A
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7655
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4400
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5848
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7405
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2569
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6082
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/1-25717207-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25717207
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25717207
    reference: chr 1
allele count: 1
allele frequency: 8.245926512302922e-6
allele num: 121272
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+33G>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.753+33G>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*132-1603G>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+11880G>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.801+33G>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.801+33G>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.487-1603G>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.753+33G>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-4872G>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.487-1603G>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.801+33G>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.801+33G>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.956+33G>T
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4400
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6084
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7648
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3780
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4702
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5848
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2572
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: DP
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

1-25717208-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25717208
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25717208
    reference: chr 1
allele count: 1
allele frequency: 8.244566830458728e-6
allele num: 121292
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.753+32G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.801+32G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-4873G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.801+32G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.801+32G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+32G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.801+32G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.753+32G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.487-1604G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.956+32G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.487-1604G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+11879G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*132-1604G>C
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4403
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3780
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4702
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1490
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2759
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7409
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6082
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7648
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum

1-25717212-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25717212
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25717212
    reference: chr 1
allele count: 1
allele frequency: 8.243071698237632e-6
allele num: 121314
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.956+28A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.753+28A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.487-1608A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.801+28A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.801+28A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.801+28A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.801+28A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.487-1608A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+11875A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+28A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*132-1608A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-4877A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.753+28A>G
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4696
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2588
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2758
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7649
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4411
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3779
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6079
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2071
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum

1-25717217-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25717217
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25717217
    reference: chr 1
allele count: 1
allele frequency: 8.241441263248117e-6
allele num: 121338
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.801+23G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.801+23G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.487-1613G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.801+23G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-4882G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.753+23G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.753+23G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*132-1613G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.487-1613G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.956+23G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.801+23G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+11870G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+23G>C
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6081
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2613
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3779
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7646
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4423
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2758
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1358
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7405
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5845
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum

1-25717218-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25717218
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25717218
    reference: chr 1
allele count: 3
allele frequency: 2.472513887286333e-5
allele num: 121334
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+11869G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.801+22G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.753+22G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.753+22G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.801+22G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.487-1614G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.487-1614G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*132-1614G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.956+22G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+22G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-4883G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.801+22G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.801+22G>A
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2758
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7646
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4427
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2071
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6080
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4695
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7404
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3779
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

1-25717219-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25717219
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25717219
    reference: chr 1
allele count: 152
allele frequency: 1.252616485092216e-3
allele num: 121346
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+11868G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.801+21G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.801+21G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+21G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.956+21G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.487-1615G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.753+21G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.487-1615G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*132-1615G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-4884G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.801+21G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.753+21G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.801+21G>C
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6064
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2077
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 7385
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 8.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 8.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 7633
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3788
  bin: 6.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 9.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 7110
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4699
  bin: 6.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 9.75e1
  variant carriers: 45
genotype quality: GenotypeQuality
num of homozygotes: 4
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

1-25717228-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25717228
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25717228
    reference: chr 1
allele count: 3
allele frequency: 2.471576866040534e-5
allele num: 121380
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.801+12G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-4893G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.956+12G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.487-1624G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.753+12G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*132-1624G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.753+12G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+11859G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.801+12G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.487-1624G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+12G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.801+12G>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.801+12G>C
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7636
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2641
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4700
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7389
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4436
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6073
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3784
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2767
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7120
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5838
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQ

1-25717228-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25717228
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25717228
    reference: chr 1
allele count: 9
allele frequency: 7.414730598121601e-5
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-4893G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.487-1624G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.956+12G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.801+12G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.487-1624G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+11859G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+12G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.753+12G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.753+12G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.801+12G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.801+12G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.801+12G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*132-1624G>A
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4700
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7636
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2767
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2641
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5838
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6073
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7120
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD

1-25717229-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25717229
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25717229
    reference: chr 1
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.801+11C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-4894C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.753+11C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.487-1625C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.956+11C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.801+11C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.801+11C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+11858C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.753+11C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.487-1625C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*132-1625C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.801+11C>T
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.801+11C>T
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4436
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7634
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4702
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3785
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7391
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5839
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6074
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7124
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2767
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2645
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

1-25717241-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25717241
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25717241
    reference: chr 1
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.955T>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.800T>C
  hgvsp: ENSP00000392809.1:p.Met267Thr
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-4906T>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.487-1637T>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.752T>C
  hgvsp: ENSP00000311185.4:p.Met251Thr
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.800T>C
  hgvsp: ENSP00000415417.1:p.Met267Thr
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.800T>C
  hgvsp: ENSP00000243186.6:p.Met267Thr
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.487-1637T>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.800T>C
  hgvsp: ENSP00000294413.6:p.Met267Thr
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.800T>C
  hgvsp: ENSP00000334570.5:p.Met267Thr
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*132-1637T>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+11846T>C
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.752T>C
  hgvsp: ENSP00000363472.2:p.Met251Thr
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6067
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7121
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3790
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4436
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7387
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7639
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2645
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5838
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met267Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD

1-25717241-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25717241
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25717241
    reference: chr 1
allele count: 41
allele frequency: 3.377933034537305e-4
allele num: 121376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.955T>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-4906T>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+11846T>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.800T>A
  hgvsp: ENSP00000415417.1:p.Met267Lys
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.487-1637T>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.752T>A
  hgvsp: ENSP00000311185.4:p.Met251Lys
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.800T>A
  hgvsp: ENSP00000334570.5:p.Met267Lys
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.800T>A
  hgvsp: ENSP00000392809.1:p.Met267Lys
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.800T>A
  hgvsp: ENSP00000294413.6:p.Met267Lys
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*132-1637T>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.487-1637T>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.800T>A
  hgvsp: ENSP00000243186.6:p.Met267Lys
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.752T>A
  hgvsp: ENSP00000363472.2:p.Met251Lys
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7121
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2645
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7639
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6067
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 9.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4436
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2766
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met267Lys
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

1-25717244-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25717244
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25717244
    reference: chr 1
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.749G>A
  hgvsp: ENSP00000363472.2:p.Ser250Asn
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+11843G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.797G>A
  hgvsp: ENSP00000294413.6:p.Ser266Asn
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-4909G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.487-1640G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*132-1640G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.797G>A
  hgvsp: ENSP00000415417.1:p.Ser266Asn
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.797G>A
  hgvsp: ENSP00000243186.6:p.Ser266Asn
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.797G>A
  hgvsp: ENSP00000334570.5:p.Ser266Asn
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.797G>A
  hgvsp: ENSP00000392809.1:p.Ser266Asn
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.487-1640G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.952G>A
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.749G>A
  hgvsp: ENSP00000311185.4:p.Ser250Asn
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7639
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2077
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4438
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2646
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2767
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7387
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4703
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser266Asn
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

1-25717254-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25717254
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25717254
    reference: chr 1
allele count: 41
allele frequency: 3.377821716922063e-4
allele num: 121380
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.787A>G
  hgvsp: ENSP00000243186.6:p.Arg263Gly
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.787A>G
  hgvsp: ENSP00000392809.1:p.Arg263Gly
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.942A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.487-1650A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.787A>G
  hgvsp: ENSP00000294413.6:p.Arg263Gly
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+11833A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.739A>G
  hgvsp: ENSP00000311185.4:p.Arg247Gly
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.787A>G
  hgvsp: ENSP00000334570.5:p.Arg263Gly
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.787A>G
  hgvsp: ENSP00000415417.1:p.Arg263Gly
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-4919A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.739A>G
  hgvsp: ENSP00000363472.2:p.Arg247Gly
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*132-1650A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.487-1650A>G
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2649
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2765
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7638
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6065
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4707
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7387
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7119
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 7.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Arg263Gly
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

1-25717255-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25717255
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 25717255
    reference: chr 1
allele count: 3
allele frequency: 2.471128976458378e-5
allele num: 121402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000431741
  ensembl transcript: ENST00000527747
  gene symbol: RHCE
  hgvsc: ENST00000527747.1:c.107+11832A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000188672
  ensembl transcript: ENST00000527187
  gene symbol: RHCE
  hgvsc: ENST00000527187.1:n.941A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000435401
  ensembl transcript: ENST00000533771
  gene symbol: RHCE
  hgvsc: ENST00000533771.1:c.*132-1651A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000392809
  ensembl transcript: ENST00000425135
  gene symbol: RHCE
  hgvsc: ENST00000425135.1:c.786A>G
  hgvsp: ENST00000425135.1:c.786A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000415417
  ensembl transcript: ENST00000413854
  gene symbol: RHCE
  hgvsc: ENST00000413854.1:c.786A>G
  hgvsp: ENST00000413854.1:c.786A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000334570
  ensembl transcript: ENST00000349438
  gene symbol: RHCE
  hgvsc: ENST00000349438.4:c.786A>G
  hgvsp: ENST00000349438.4:c.786A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000294413
  ensembl transcript: ENST00000294413
  gene symbol: RHCE
  hgvsc: ENST00000294413.7:c.786A>G
  hgvsp: ENST00000294413.7:c.786A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000363472
  ensembl transcript: ENST00000374352
  gene symbol: RHCE
  hgvsc: ENST00000374352.2:c.738A>G
  hgvsp: ENST00000374352.2:c.738A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000243186
  ensembl transcript: ENST00000243186
  gene symbol: RHCE
  hgvsc: ENST00000243186.6:c.786A>G
  hgvsp: ENST00000243186.6:c.786A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000311185
  ensembl transcript: ENST00000349320
  gene symbol: RHCE
  hgvsc: ENST00000349320.3:c.738A>G
  hgvsp: ENST00000349320.3:c.738A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000344485
  ensembl transcript: ENST00000346452
  gene symbol: RHCE
  hgvsc: ENST00000346452.4:c.487-4920A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000416275
  ensembl transcript: ENST00000455194
  gene symbol: RHCE
  hgvsc: ENST00000455194.1:c.487-1651A>G
  variant of: http://identifiers.org/hgnc/10008
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188672
  ensembl protein: ENSP00000345084
  ensembl transcript: ENST00000340849
  gene symbol: RHCE
  hgvsc: ENST00000340849.4:c.487-1651A>G
  variant of: http://identifiers.org/hgnc/10008
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3783
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4438
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6066
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4708
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7636
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7386
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2647
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5837
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln262Gln
num of homozygotes: 0
population: African
reference allele: T

GenotypeDepth
all individuals: 599
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4163
bin: 9.25e1
variant carriers: 8

GenotypeDepth
all individuals: 896
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4888
bin: 8.25e1
variant carriers: 5

GenotypeDepth
all individuals: 1224
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 4580
bin: 7.25e1
variant carriers: 3

GenotypeDepth
all individuals: 4127
bin: 6.75e1
variant carriers: 2

GenotypeDepth
all individuals: 1716
bin: 4.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 1
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 58236
bin: 9.75e1
variant carriers: 232

GenotypeQuality
all individuals: 212
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 569
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 290
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 8
allele frequency: 6.909656244601831e-4
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 8.990110878034162e-5
allele num: 66740
num of homozygotes: 0

African
type: Population
allele count: 217
allele frequency: 2.085335383432635e-2
allele num: 10406
num of homozygotes: 1

Other
type: Population
allele count: 2
allele frequency: 2.202643171806168e-3
allele num: 908
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.22e-2

FS
type: SiteQuality
SIO_000300: 5.47e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.141e0

MQ
type: SiteQuality
SIO_000300: 5.293e1

VQSLOD
type: SiteQuality
SIO_000300: -3.135e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.86e0

DP
type: SiteQuality
SIO_000300: 5.20546e6

QD
type: SiteQuality
SIO_000300: 1.31e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.33e-1

GenotypeDepth
all individuals: 4164
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 599
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 896
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 392
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 568
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 353
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 58230
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 210
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

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

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

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 2.675e0

MQ
type: SiteQuality
SIO_000300: 5.08e1

DP
type: SiteQuality
SIO_000300: 5.190871e6

VQSLOD
type: SiteQuality
SIO_000300: -1.168e0

MQRankSum
type: SiteQuality
SIO_000300: 3.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.1e0

QD
type: SiteQuality
SIO_000300: 1.705e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.13e-1

GenotypeDepth
all individuals: 4668
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4164
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4631
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 568
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 392
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58228
bin: 9.75e1
variant carriers: 1

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.14e0

MQ
type: SiteQuality
SIO_000300: 5.127e1

VQSLOD
type: SiteQuality
SIO_000300: -6.086e-1

InbreedingCoeff
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SIO_000300: 0.0e0

ReadPosRankSum
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SIO_000300: -8.1e-2

FS
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SIO_000300: 1.349e0

ClippingRankSum
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SIO_000300: 2.43e-1

BaseQRankSum
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SIO_000300: -8.31e-1

DP
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SIO_000300: 5.190793e6

QD
type: SiteQuality
SIO_000300: 8.83e0

GenotypeDepth
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variant carriers: 1

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

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

East Asian
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allele count: 3
allele frequency: 3.467406380027739e-4
allele num: 8652
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

Other
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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: 10406
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

South Asian
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ClippingRankSum
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SIO_000300: -2.48e-1

VQSLOD
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FS
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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DP
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SIO_000300: 5.190688e6

MQRankSum
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SIO_000300: 5.11e-1

MQ
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SIO_000300: 5.378e1

QD
type: SiteQuality
SIO_000300: 1.227e1

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

Latino
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allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

East Asian
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allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 5.190453e6

MQ
type: SiteQuality
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MQRankSum
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FS
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SIO_000300: 4.238e0

VQSLOD
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BaseQRankSum
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SIO_000300: -8.9e-2

InbreedingCoeff
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SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: 1.0e0

QD
type: SiteQuality
SIO_000300: 8.15e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.68e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

Latino
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allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 5.190439e6

FS
type: SiteQuality
SIO_000300: 4.403e0

InbreedingCoeff
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SIO_000300: 0.0e0

MQRankSum
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BaseQRankSum
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MQ
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SIO_000300: 5.355e1

VQSLOD
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SIO_000300: -2.09e0

QD
type: SiteQuality
SIO_000300: 7.32e0

ClippingRankSum
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SIO_000300: -1.186e0

ReadPosRankSum
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SIO_000300: 1.9e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

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

Other
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.47e0

InbreedingCoeff
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SIO_000300: 0.0e0

ReadPosRankSum
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FS
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QD
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MQ
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BaseQRankSum
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DP
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VQSLOD
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ClippingRankSum
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SIO_000300: -6.45e-1

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10394
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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 frequency: 0.0e0
allele num: 66638
num of homozygotes: 0

South Asian
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East Asian
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Other
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allele num: 904
num of homozygotes: 0

FS
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QD
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MQRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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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: 2

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 38

African
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allele frequency: 3.270488649480569e-3
allele num: 10396
num of homozygotes: 0

East Asian
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Other
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.000300030003e-5
allele num: 66660
num of homozygotes: 0

Latino
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allele num: 11550
num of homozygotes: 0

European (Finnish)
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South Asian
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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FS
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DP
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MQ
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QD
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1.211680600993578e-4
allele num: 16506
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66696
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East Asian
type: Population
allele count: 0
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ReadPosRankSum
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SIO_000300: 6.79e-1

DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

QD
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ClippingRankSum
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SIO_000300: 6.52e-1

VQSLOD
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MQ
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InbreedingCoeff
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SIO_000300: -1.0e-4

MQRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499115521842113e-5
allele num: 66706
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498890820792613e-5
allele num: 66716
num of homozygotes: 0

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

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

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

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

European (Finnish)
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allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 4.18e-1

ClippingRankSum
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BaseQRankSum
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QD
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FS
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MQ
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MQRankSum
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InbreedingCoeff
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SIO_000300: -1.0e-4

DP
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SIO_000300: 1.97744e6

VQSLOD
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SIO_000300: -1.25e0

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

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

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

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

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

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

African
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allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

East Asian
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allele frequency: 1.157407407407407e-4
allele num: 8640
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 4.211e1

VQSLOD
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 2.2575e1

ReadPosRankSum
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SIO_000300: 3.08e-1

DP
type: SiteQuality
SIO_000300: 1.980554e6

QD
type: SiteQuality
SIO_000300: 1.4e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.5e-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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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 1
allele frequency: 8.650519031141868e-5
allele num: 11560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66702
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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East Asian
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African
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Other
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MQRankSum
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VQSLOD
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QD
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BaseQRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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MQ
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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 num: 16512
num of homozygotes: 0

East Asian
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African
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Latino
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num of homozygotes: 0

European (Finnish)
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Other
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European (Non-Finnish)
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allele frequency: 4.497211728728189e-5
allele num: 66708
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ReadPosRankSum
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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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VQSLOD
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QD
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DP
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BaseQRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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European (Non-Finnish)
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num of homozygotes: 0

Latino
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allele frequency: 1.731301939058172e-4
allele num: 11552
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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South Asian
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East Asian
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FS
type: SiteQuality
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MQRankSum
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DP
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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QD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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South Asian
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European (Finnish)
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East Asian
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European (Non-Finnish)
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BaseQRankSum
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DP
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InbreedingCoeff
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MQRankSum
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VQSLOD
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MQ
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FS
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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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East Asian
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European (Finnish)
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European (Non-Finnish)
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DP
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MQ
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FS
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MQRankSum
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QD
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BaseQRankSum
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InbreedingCoeff
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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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African
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East Asian
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Latino
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European (Non-Finnish)
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FS
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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MQ
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QD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Finnish)
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European (Non-Finnish)
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South Asian
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FS
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ReadPosRankSum
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QD
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BaseQRankSum
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MQRankSum
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MQ
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DP
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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European (Finnish)
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African
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Other
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European (Non-Finnish)
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East Asian
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QD
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DP
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ClippingRankSum
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InbreedingCoeff
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MQ
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FS
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MQRankSum
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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South Asian
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African
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East Asian
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VQSLOD
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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QD
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DP
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FS
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MQ
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GenotypeDepth
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GenotypeQuality
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Latino
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African
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European (Non-Finnish)
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South Asian
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ClippingRankSum
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DP
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FS
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MQ
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VQSLOD
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QD
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MQRankSum
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BaseQRankSum
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SIO_000300: 2.02e-1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499430216517723e-5
allele num: 66692
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 904
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 frequency: 0.0e0
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num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8642
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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500195025353296e-5
allele num: 66658
num of homozygotes: 0

South Asian
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allele count: 0
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num of homozygotes: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
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InbreedingCoeff
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SIO_000300: -5.0e-4

ClippingRankSum
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SIO_000300: 5.01e-1

VQSLOD
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ReadPosRankSum
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MQ
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SIO_000300: 4.001e1

QD
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FS
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SIO_000300: 2.537e0

MQRankSum
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SIO_000300: -1.33e-1

BaseQRankSum
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SIO_000300: -5.91e-1

DP
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SIO_000300: 1.978092e6

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16478
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
type: Population
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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: 9
allele frequency: 1.389317690645261e-4
allele num: 64780
num of homozygotes: 0

African
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allele count: 1
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num of homozygotes: 0

Latino
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allele num: 11394
num of homozygotes: 0

East Asian
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allele count: 2
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allele num: 8524
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MQRankSum
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SIO_000300: -5.46e-1

DP
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QD
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InbreedingCoeff
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FS
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SIO_000300: 2.52775e2

MQ
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ReadPosRankSum
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BaseQRankSum
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SIO_000300: -2.993e0

VQSLOD
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SIO_000300: -3.043e2

ClippingRankSum
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SIO_000300: 3.99e0

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

East Asian
type: Population
allele count: 0
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num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
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allele num: 66714
num of homozygotes: 0

European (Finnish)
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FS
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QD
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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VQSLOD
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DP
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InbreedingCoeff
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

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

African
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Latino
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num of homozygotes: 0

Other
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European (Finnish)
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South Asian
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East Asian
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QD
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FS
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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DP
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MQ
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MQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1
allele frequency: 1.499205421126803e-5
allele num: 66702
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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East Asian
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Other
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Latino
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South Asian
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QD
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ClippingRankSum
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MQRankSum
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
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MQ
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DP
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GenotypeDepth
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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

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: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 2.999400119976005e-5
allele num: 66680
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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East Asian
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allele frequency: 2.313208420078649e-3
allele num: 8646
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African
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allele frequency: 0.0e0
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Latino
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South Asian
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MQRankSum
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BaseQRankSum
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FS
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SIO_000300: 5.3e-1

MQ
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DP
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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QD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 3
allele frequency: 2.889616644191871e-4
allele num: 10382
num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 904
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Latino
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allele frequency: 0.0e0
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East Asian
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allele frequency: 1.156871818602499e-4
allele num: 8644
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 2.999580058791769e-5
allele num: 66676
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DP
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SIO_000300: 1.96146e6

BaseQRankSum
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InbreedingCoeff
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FS
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MQRankSum
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MQ
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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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: 1
allele frequency: 1.503397678753984e-5
allele num: 66516
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 1.505706628120577e-5
allele num: 66414
num of homozygotes: 0

South Asian
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African
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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

MQRankSum
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SIO_000300: -1.07e-1

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

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

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

Latino
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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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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.012048192771084e-5
allele num: 66400
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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VQSLOD
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ReadPosRankSum
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FS
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QD
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ClippingRankSum
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MQ
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DP
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SIO_000300: 1.935549e6

GenotypeDepth
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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 count: 1
allele frequency: 9.706853038245001e-5
allele num: 10302
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6434
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.510665296996797e-5
allele num: 66196
num of homozygotes: 0

Other
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num of homozygotes: 0

Latino
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QD
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ReadPosRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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FS
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MQRankSum
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SIO_000300: -1.54e-1

BaseQRankSum
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SIO_000300: 3.09e0

DP
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ClippingRankSum
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SIO_000300: 1.55e-1

GenotypeDepth
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variant carriers: 4

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

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

South Asian
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allele count: 3
allele frequency: 1.821272462360369e-4
allele num: 16472
num of homozygotes: 0

Latino
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allele count: 4
allele frequency: 3.500175008750437e-4
allele num: 11428
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.538715241005779e-5
allele num: 66098
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 26
allele frequency: 2.525252525252525e-3
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ClippingRankSum
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QD
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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FS
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DP
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MQ
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InbreedingCoeff
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SIO_000300: 6.1e-3

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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European (Non-Finnish)
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allele num: 65796
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East Asian
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Other
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Latino
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European (Finnish)
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MQRankSum
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QD
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ReadPosRankSum
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DP
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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FS
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MQ
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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Other
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Latino
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African
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European (Non-Finnish)
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South Asian
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East Asian
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ReadPosRankSum
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MQ
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VQSLOD
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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DP
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ClippingRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 (Non-Finnish)
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South Asian
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Other
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6348
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.058e0

InbreedingCoeff
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SIO_000300: 1.5e-3

DP
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SIO_000300: 1.904153e6

MQ
type: SiteQuality
SIO_000300: 3.128e1

BaseQRankSum
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SIO_000300: 4.76e0

ClippingRankSum
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SIO_000300: -5.4e-2

MQRankSum
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SIO_000300: 7.27e-1

ReadPosRankSum
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SIO_000300: 1.04e-1

FS
type: SiteQuality
SIO_000300: 2.095e0

QD
type: SiteQuality
SIO_000300: 1.301e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7998
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63264
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10722
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6030
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.172077521293668e-5
allele num: 16202
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9846
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.780951e6

MQ
type: SiteQuality
SIO_000300: 3.079e1

FS
type: SiteQuality
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ReadPosRankSum
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QD
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MQRankSum
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SIO_000300: 1.35e0

InbreedingCoeff
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SIO_000300: 1.4e-3

BaseQRankSum
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SIO_000300: 5.06e0

VQSLOD
type: SiteQuality
SIO_000300: -8.769e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.6e-1

GenotypeDepth
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variant carriers: 10

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6032
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.16716285551403e-5
allele num: 63148
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.017708121310808e-4
allele num: 9826
num of homozygotes: 0

East Asian
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allele count: 13
allele frequency: 1.630707476166583e-3
allele num: 7972
num of homozygotes: 0

South Asian
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allele count: 39
allele frequency: 2.408596837944664e-3
allele num: 16192
num of homozygotes: 0

Other
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allele count: 1
allele frequency: 1.16822429906542e-3
allele num: 856
num of homozygotes: 0

Latino
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allele count: 3
allele frequency: 2.801643630930146e-4
allele num: 10708
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.269e1

InbreedingCoeff
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SIO_000300: -5.999999999999999e-4

MQRankSum
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BaseQRankSum
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SIO_000300: -2.507e0

ReadPosRankSum
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SIO_000300: 3.11e-1

MQ
type: SiteQuality
SIO_000300: 3.115e1

VQSLOD
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SIO_000300: -3.189e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.28e-1

DP
type: SiteQuality
SIO_000300: 1.770104e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 7327
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variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9716
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7772
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62202
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16110
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5910
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.562057754828839e-5
allele num: 10458
num of homozygotes: 0

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

MQRankSum
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SIO_000300: -1.55e0

VQSLOD
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ReadPosRankSum
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SIO_000300: -1.022e0

MQ
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SIO_000300: 3.168e1

DP
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SIO_000300: 1.686684e6

InbreedingCoeff
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SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: 4.29e-1

QD
type: SiteQuality
SIO_000300: 1.207e1

BaseQRankSum
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SIO_000300: -3.989e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 668
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59726
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5556
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 1
allele frequency: 6.300403225806451e-5
allele num: 15872
num of homozygotes: 0

ClippingRankSum
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SIO_000300: -2.71e-1

MQ
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FS
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QD
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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VQSLOD
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DP
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SIO_000300: 1.445038e6

ReadPosRankSum
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SIO_000300: 8.129999999999999e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5484
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.387878171900939e-5
allele num: 59034
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
SIO_000300: -3.01e0

FS
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BaseQRankSum
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MQRankSum
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DP
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QD
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ClippingRankSum
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InbreedingCoeff
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MQ
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 4

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
type: Population
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num of homozygotes: 0

African
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allele frequency: 1.435512367491166e-3
allele num: 9056
num of homozygotes: 0

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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East Asian
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South Asian
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ClippingRankSum
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MQ
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BaseQRankSum
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VQSLOD
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MQRankSum
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FS
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InbreedingCoeff
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 1
allele frequency: 9.620935154897056e-5
allele num: 10394
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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South Asian
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European (Non-Finnish)
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European (Finnish)
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East Asian
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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MQ
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VQSLOD
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QD
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FS
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ClippingRankSum
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InbreedingCoeff
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Other
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East Asian
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African
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Latino
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European (Non-Finnish)
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European (Finnish)
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MQRankSum
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DP
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QD
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MQ
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VQSLOD
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ClippingRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 66668
num of homozygotes: 0

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

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

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

Latino
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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

African
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allele frequency: 2.886836027713626e-4
allele num: 10392
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East 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 frequency: 0.0e0
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DP
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SIO_000300: 3.190723e6

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

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

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

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

Other
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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 2.998590662388677e-5
allele num: 66698
num of homozygotes: 0

Latino
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allele frequency: 5.185825410544512e-4
allele num: 11570
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 1.385148133897653e-2
allele num: 10396
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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QD
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FS
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DP
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InbreedingCoeff
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

Other
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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.49599856128046e-5
allele num: 66726
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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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allele frequency: 0.0e0
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East Asian
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VQSLOD
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
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ClippingRankSum
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QD
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DP
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MQ
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SIO_000300: 5.476e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 9

GenotypeQuality
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variant carriers: 0

Latino
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allele count: 7
allele frequency: 6.049083995852057e-4
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

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

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

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

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

African
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South Asian
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East Asian
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Latino
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Other
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European (Non-Finnish)
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MQRankSum
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InbreedingCoeff
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QD
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MQ
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ClippingRankSum
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DP
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ReadPosRankSum
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BaseQRankSum
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FS
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VQSLOD
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GenotypeDepth
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variant carriers: 2

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

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

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

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

GenotypeQuality
all individuals: 2629
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2579
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1738
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1436
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2142
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1622
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.381e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -9.84e-1

MQ
type: SiteQuality
SIO_000300: 5.634e1

DP
type: SiteQuality
SIO_000300: 3.197983e6

QD
type: SiteQuality
SIO_000300: 7.7e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.977e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.93e-1

FS
type: SiteQuality
SIO_000300: 4.864e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.95e-1

GenotypeDepth
all individuals: 1546
bin: 9.75e1
variant carriers: 21

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

GenotypeDepth
all individuals: 4438
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3782
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5838
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1009
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2140
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47529
bin: 9.75e1
variant carriers: 39

GenotypeQuality
all individuals: 2577
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2627
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1735
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1624
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1436
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 2

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

East Asian
type: Population
allele count: 3
allele frequency: 3.466605038132656e-4
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495459585818323e-5
allele num: 66734
num of homozygotes: 0

African
type: Population
allele count: 35
allele frequency: 3.370570107858243e-3
allele num: 10384
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -4.606e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.589e0

QD
type: SiteQuality
SIO_000300: 6.31e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.42e0

VQSLOD
type: SiteQuality
SIO_000300: -3.818e0

FS
type: SiteQuality
SIO_000300: 1.472e0

DP
type: SiteQuality
SIO_000300: 3.199575e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.202e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.102e0

GenotypeDepth
all individuals: 1548
bin: 9.75e1
variant carriers: 3

GenotypeDepth
all individuals: 7119
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 746
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2077
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2767
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2627
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1624
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2139
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1736
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1438
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2577
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1010
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47547
bin: 9.75e1
variant carriers: 3

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