22-20113904-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20113904
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20113904
    reference: chr 22
allele count: 1
allele frequency: 8.459091831900928e-6
allele num: 118216
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+13C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*610C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000404298
  ensembl transcript: ENST00000423859
  gene symbol: RANBP1
  hgvsc: ENST00000423859.1:c.368C>T
  hgvsp: ENSP00000404298.1:p.Pro123Leu
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+13C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.248C>T
  hgvsp: ENSP00000401564.1:p.Pro83Leu
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1377C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+13C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+13C>T
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7697
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29203
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18950
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2335
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro123Leu
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD

22-20113911-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20113911
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20113910
    reference: chr 22
allele count: 1
allele frequency: 8.559298822240482e-6
allele num: 116832
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000404298
  ensembl transcript: ENST00000423859
  gene symbol: RANBP1
  hgvsc: ENST00000423859.1:c.381delG
  hgvsp: ENSP00000404298.1:p.Leu128PhefsTer9
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*623delG
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+26delG
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.261delG
  hgvsp: ENSP00000401564.1:p.Leu88PhefsTer9
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+26delG
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+26delG
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+26delG
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1390delG
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 7270
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18871
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2059
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28193
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 544
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 509
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6453
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu128PhefsTer9
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: TG
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

22-20113917-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20113917
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20113917
    reference: chr 22
allele count: 2
allele frequency: 1.733943681509225e-5
allele num: 115344
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*623G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+26G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1390G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+26G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.261G>A
  hgvsp: ENST00000430524.1:c.261G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000404298
  ensembl transcript: ENST00000423859
  gene symbol: RANBP1
  hgvsc: ENST00000423859.1:c.381G>A
  hgvsp: ENST00000423859.1:c.381G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+26G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+26G>A
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2774
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18936
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2769
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27024
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6694
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42562
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1348
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 654
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly127Gly
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ

22-20113923-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20113923
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20113923
    reference: chr 22
allele count: 2
allele frequency: 1.759974656364948e-5
allele num: 113638
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+32T>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1396T>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.267T>C
  hgvsp: ENST00000430524.1:c.267T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+32T>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*629T>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+32T>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+32T>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000404298
  ensembl transcript: ENST00000423859
  gene symbol: RANBP1
  hgvsc: ENST00000423859.1:c.387T>C
  hgvsp: ENST00000423859.1:c.387T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3576
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3738
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6132
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18861
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25690
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6079
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41078
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5670
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 661
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu129Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

22-20113924-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20113924
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20113924
    reference: chr 22
allele count: 1
allele frequency: 8.825502171073534e-6
allele num: 113308
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+33T>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1397T>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+33T>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.268T>C
  hgvsp: ENSP00000401564.1:p.Cys90Arg
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000404298
  ensembl transcript: ENST00000423859
  gene symbol: RANBP1
  hgvsc: ENST00000423859.1:c.388T>C
  hgvsp: ENSP00000404298.1:p.Cys130Arg
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+33T>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+33T>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*630T>C
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25423
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3742
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18807
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6056
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1705
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3917
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6354
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1227
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40671
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 515
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Cys130Arg
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

22-20113940-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20113940
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20113940
    reference: chr 22
allele count: 1
allele frequency: 9.457874626413952e-6
allele num: 105732
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+49A>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000404298
  ensembl transcript: ENST00000423859
  gene symbol: RANBP1
  hgvsc: ENST00000423859.1:c.404A>G
  hgvsp: ENSP00000404298.1:p.His135Arg
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1413A>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*646A>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.284A>G
  hgvsp: ENSP00000401564.1:p.His95Arg
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+49A>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+49A>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000264346
  ensembl transcript: ENST00000578179
  gene symbol: SNORA77
  hgvsc: ENST00000578179.1:n.16A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+49A>G
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4263
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7306
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17702
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7469
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20097
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2942
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 385
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12131
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 520
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
hgvs: p.His135Arg
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ

22-20113948-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20113948
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20113948
    reference: chr 22
allele count: 1
allele frequency: 9.921619208254787e-6
allele num: 100790
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000264346
  ensembl transcript: ENST00000578179
  gene symbol: SNORA77
  hgvsc: ENST00000578179.1:n.24A>G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*654A>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000404298
  ensembl transcript: ENST00000423859
  gene symbol: RANBP1
  hgvsc: ENST00000423859.1:c.412A>G
  hgvsp: ENSP00000404298.1:p.Ile138Val
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+57A>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+57A>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.292A>G
  hgvsp: ENSP00000401564.1:p.Ile98Val
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1421A>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+57A>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+57A>G
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3436
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9622
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3883
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16136
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9930
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16765
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2177
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29541
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ile138Val
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

22-20113953-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20113953
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20113953
    reference: chr 22
allele count: 6
allele frequency: 6.238303181534623e-5
allele num: 96180
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000404298
  ensembl transcript: ENST00000423859
  gene symbol: RANBP1
  hgvsc: ENST00000423859.1:c.417T>G
  hgvsp: ENST00000423859.1:c.417T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1426T>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.297T>G
  hgvsp: ENST00000430524.1:c.297T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+62T>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000264346
  ensembl transcript: ENST00000578179
  gene symbol: SNORA77
  hgvsc: ENST00000578179.1:n.29T>G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*659T>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+62T>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+62T>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+62T>G
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4817
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13402
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11687
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15427
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11797
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2584
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 511
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 815
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu99Leu
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

22-20113953-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20113953
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20113952
    reference: chr 22
allele count: 4
allele frequency: 4.158868787689748e-5
allele num: 96180
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1428delC
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000404298
  ensembl transcript: ENST00000423859
  gene symbol: RANBP1
  hgvsc: ENST00000423859.1:c.419delC
  hgvsp: ENSP00000404298.1:p.Pro140GlnfsTer24
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+64delC
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.299delC
  hgvsp: ENSP00000401564.1:p.Pro100GlnfsTer24
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*661delC
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000264346
  ensembl transcript: ENST00000578179
  gene symbol: SNORA77
  hgvsc: ENST00000578179.1:n.31delC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+64delC
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+64delC
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+64delC
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13402
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11687
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11797
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2584
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15427
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4817
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1203
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1692
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2844
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Pro100GlnfsTer24
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: TC
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

22-20113959-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20113959
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20113959
    reference: chr 22
allele count: 1
allele frequency: 1.073053480985492e-5
allele num: 93192
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+68C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000404298
  ensembl transcript: ENST00000423859
  gene symbol: RANBP1
  hgvsc: ENST00000423859.1:c.423C>T
  hgvsp: ENST00000423859.1:c.423C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+68C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+68C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1432C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000264346
  ensembl transcript: ENST00000578179
  gene symbol: SNORA77
  hgvsc: ENST00000578179.1:n.35C>T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*665C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+68C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.303C>T
  hgvsp: ENST00000430524.1:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12906
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15685
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12556
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4863
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11605
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2053
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1071
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1103
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 779
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly141Gly
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: East Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

22-20113960-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20113960
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20113960
    reference: chr 22
allele count: 1
allele frequency: 1.083329722234259e-5
allele num: 92308
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+69G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+69G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+69G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*666G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000404298
  ensembl transcript: ENST00000423859
  gene symbol: RANBP1
  hgvsc: ENST00000423859.1:c.424G>A
  hgvsp: ENSP00000404298.1:p.Gly142Arg
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.304G>A
  hgvsp: ENSP00000401564.1:p.Gly102Arg
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+69G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1433G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000264346
  ensembl transcript: ENST00000578179
  gene symbol: SNORA77
  hgvsc: ENST00000578179.1:n.36G>A
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4865
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11207
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13251
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15629
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12768
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 554
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20889
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1076
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 828
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2066
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gly142Arg
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ

22-20113964-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20113964
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20113964
    reference: chr 22
allele count: 1
allele frequency: 1.121830827911151e-5
allele num: 89140
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000264346
  ensembl transcript: ENST00000578179
  gene symbol: SNORA77
  hgvsc: ENST00000578179.1:n.40G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1437G>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000404298
  ensembl transcript: ENST00000423859
  gene symbol: RANBP1
  hgvsc: ENST00000423859.1:c.428G>T
  hgvsp: ENSP00000404298.1:p.Cys143Phe
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*670G>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+73G>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+73G>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+73G>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+73G>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.308G>T
  hgvsp: ENSP00000401564.1:p.Cys103Phe
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14950
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13625
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9437
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1592
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14834
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 495
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 907
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 587
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Cys143Phe
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff

22-20113965-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20113965
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20113965
    reference: chr 22
allele count: 1
allele frequency: 1.144190942584499e-5
allele num: 87398
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.309C>G
  hgvsp: ENSP00000401564.1:p.Cys103Trp
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000404298
  ensembl transcript: ENST00000423859
  gene symbol: RANBP1
  hgvsc: ENST00000423859.1:c.429C>G
  hgvsp: ENSP00000404298.1:p.Cys143Trp
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+74C>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*671C>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+74C>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1438C>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000264346
  ensembl transcript: ENST00000578179
  gene symbol: SNORA77
  hgvsc: ENST00000578179.1:n.41C>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+74C>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+74C>G
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14569
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5265
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13978
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15373
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8796
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 385
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1588
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 847
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Cys143Trp
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

22-20113966-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20113966
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20113966
    reference: chr 22
allele count: 1
allele frequency: 1.1441647597254e-5
allele num: 87400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+75T>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+75T>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*672T>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+75T>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000264346
  ensembl transcript: ENST00000578179
  gene symbol: SNORA77
  hgvsc: ENST00000578179.1:n.42T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.310T>C
  hgvsp: ENSP00000401564.1:p.Phe104Leu
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000404298
  ensembl transcript: ENST00000423859
  gene symbol: RANBP1
  hgvsc: ENST00000423859.1:c.430T>C
  hgvsp: ENSP00000404298.1:p.Phe144Leu
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+75T>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1439T>C
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8758
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14708
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15496
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1458
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13952
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5111
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1159
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19303
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2992
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2125
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Phe144Leu
num of homozygotes: 0
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

22-20113971-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20113971
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20113971
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 85476
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+80C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000264346
  ensembl transcript: ENST00000578179
  gene symbol: SNORA77
  hgvsc: ENST00000578179.1:n.47C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+80C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*677C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.315C>T
  hgvsp: ENST00000430524.1:c.315C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+80C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+80C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000404298
  ensembl transcript: ENST00000423859
  gene symbol: RANBP1
  hgvsc: ENST00000423859.1:c.435C>T
  hgvsp: ENST00000423859.1:c.435C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1444C>T
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 14318
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16427
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5008
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7881
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14431
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18588
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3055
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Phe145Phe
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD

22-20113974-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20113974
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20113974
    reference: chr 22
allele count: 3
allele frequency: 3.558634433346777e-5
allele num: 84302
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+83T>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+83T>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+83T>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*680T>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1447T>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000404298
  ensembl transcript: ENST00000423859
  gene symbol: RANBP1
  hgvsc: ENST00000423859.1:c.438T>C
  hgvsp: ENST00000423859.1:c.438T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000264346
  ensembl transcript: ENST00000578179
  gene symbol: SNORA77
  hgvsc: ENST00000578179.1:n.50T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+83T>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.318T>C
  hgvsp: ENST00000430524.1:c.318T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7299
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4868
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17096
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14273
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14532
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1783
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2088
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Cys146Cys
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: QD

22-20113976-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20113976
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20113976
    reference: chr 22
allele count: 2
allele frequency: 2.400729821865847e-5
allele num: 83308
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+85T>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+85T>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.320T>A
  hgvsp: ENSP00000401564.1:p.Leu107Gln
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1449T>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*682T>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000404298
  ensembl transcript: ENST00000423859
  gene symbol: RANBP1
  hgvsc: ENST00000423859.1:c.440T>A
  hgvsp: ENSP00000404298.1:p.Leu147Gln
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+85T>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+85T>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000264346
  ensembl transcript: ENST00000578179
  gene symbol: SNORA77
  hgvsc: ENST00000578179.1:n.52T>A
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14715
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17527
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14036
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4764
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7007
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 900
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3133
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17873
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Leu147Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

22-20113993-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20113993
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20113993
    reference: chr 22
allele count: 1
allele frequency: 1.34603995046573e-5
allele num: 74292
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+102A>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.337A>G
  hgvsp: ENSP00000401564.1:p.Arg113Gly
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000404298
  ensembl transcript: ENST00000423859
  gene symbol: RANBP1
  hgvsc: ENST00000423859.1:c.457A>G
  hgvsp: ENSP00000404298.1:p.Arg153Gly
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*699A>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+102A>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+102A>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1466A>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000264346
  ensembl transcript: ENST00000578179
  gene symbol: SNORA77
  hgvsc: ENST00000578179.1:n.69A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+102A>G
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4179
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16014
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5299
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10946
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1798
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30342
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg153Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum

22-20113999-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20113999
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20113999
    reference: chr 22
allele count: 1
allele frequency: 1.435173225408307e-5
allele num: 69678
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+108C>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000264346
  ensembl transcript: ENST00000578179
  gene symbol: SNORA77
  hgvsc: ENST00000578179.1:n.75C>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000404298
  ensembl transcript: ENST00000423859
  gene symbol: RANBP1
  hgvsc: ENST00000423859.1:c.463C>G
  hgvsp: ENSP00000404298.1:p.Leu155Val
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+108C>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.343C>G
  hgvsp: ENSP00000401564.1:p.Leu115Val
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1472C>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*705C>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+108C>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+108C>G
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16127
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2313
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22695
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9677
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1737
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31087
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Leu155Val
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

22-20114006-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114006
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114006
    reference: chr 22
allele count: 2
allele frequency: 3.046180090166931e-5
allele num: 65656
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+115C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000404298
  ensembl transcript: ENST00000423859
  gene symbol: RANBP1
  hgvsc: ENST00000423859.1:c.470C>T
  hgvsp: ENSP00000404298.1:p.Pro157Leu
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.350C>T
  hgvsp: ENSP00000401564.1:p.Pro117Leu
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+115C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*712C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1479C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000264346
  ensembl transcript: ENST00000578179
  gene symbol: SNORA77
  hgvsc: ENST00000578179.1:n.82C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+115C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+115C>T
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9267
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24212
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2789
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3495
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15622
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4105
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 474
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1744
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro157Leu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

22-20114007-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114007
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114007
    reference: chr 22
allele count: 5
allele frequency: 7.735866571773371e-5
allele num: 64634
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*713G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000264346
  ensembl transcript: ENST00000578179
  gene symbol: SNORA77
  hgvsc: ENST00000578179.1:n.83G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000404298
  ensembl transcript: ENST00000423859
  gene symbol: RANBP1
  hgvsc: ENST00000423859.1:c.471G>A
  hgvsp: ENST00000423859.1:c.471G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+116G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.351G>A
  hgvsp: ENST00000430524.1:c.351G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1480G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+116G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+116G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+116G>A
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4057
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24442
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9259
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3389
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15515
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2846
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2818
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro157Pro
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

22-20114013-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114013
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114013
    reference: chr 22
allele count: 4
allele frequency: 6.452029163171818e-5
allele num: 61996
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+122C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+122C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000404298
  ensembl transcript: ENST00000423859
  gene symbol: RANBP1
  hgvsc: ENST00000423859.1:c.477C>T
  hgvsp: ENST00000423859.1:c.477C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+122C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*719C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.357C>T
  hgvsp: ENST00000430524.1:c.357C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000264346
  ensembl transcript: ENST00000578179
  gene symbol: SNORA77
  hgvsc: ENST00000578179.1:n.89C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1486C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+122C>T
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25611
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9164
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3333
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14877
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2728
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3822
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2307
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1193
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
hgvs: p.His159His
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

22-20114014-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114014
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114014
    reference: chr 22
allele count: 4
allele frequency: 6.557592052198433e-5
allele num: 60998
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+123G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000404298
  ensembl transcript: ENST00000423859
  gene symbol: RANBP1
  hgvsc: ENST00000423859.1:c.478G>A
  hgvsp: ENSP00000404298.1:p.Val160Ile
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*720G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000264346
  ensembl transcript: ENST00000578179
  gene symbol: SNORA77
  hgvsc: ENST00000578179.1:n.90G>A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+123G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.358G>A
  hgvsp: ENSP00000401564.1:p.Val120Ile
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+123G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1487G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+123G>A
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3745
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8990
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25873
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2627
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14803
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3508
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10804
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 914
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1583
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val160Ile
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD

22-20114014-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114014
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114014
    reference: chr 22
allele count: 2
allele frequency: 3.278796026099216e-5
allele num: 60998
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000404298
  ensembl transcript: ENST00000423859
  gene symbol: RANBP1
  hgvsc: ENST00000423859.1:c.478G>T
  hgvsp: ENSP00000404298.1:p.Val160Leu
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*720G>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+123G>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000264346
  ensembl transcript: ENST00000578179
  gene symbol: SNORA77
  hgvsc: ENST00000578179.1:n.90G>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+123G>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+123G>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1487G>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+123G>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.358G>T
  hgvsp: ENSP00000401564.1:p.Val120Leu
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3745
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2627
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8990
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3508
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14803
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25873
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2613
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1583
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val160Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
reference allele: G
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

22-20114028-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114028
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114028
    reference: chr 22
allele count: 1
allele frequency: 1.839114282561518e-5
allele num: 54374
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+137G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*734G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000404298
  ensembl transcript: ENST00000423859
  gene symbol: RANBP1
  hgvsc: ENST00000423859.1:c.492G>A
  hgvsp: ENSP00000404298.1:p.Met164Ile
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+137G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000264346
  ensembl transcript: ENST00000578179
  gene symbol: SNORA77
  hgvsc: ENST00000578179.1:n.104G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+137G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.372G>A
  hgvsp: ENSP00000401564.1:p.Met124Ile
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1501G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+137G>A
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3339
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7811
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13866
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27205
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5428
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2122
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9572
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2273
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Met164Ile
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

22-20114063-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114063
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114063
    reference: chr 22
allele count: 7
allele frequency: 1.885267977376784e-4
allele num: 37130
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+172C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1536C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000404298
  ensembl transcript: ENST00000423859
  gene symbol: RANBP1
  hgvsc: ENST00000423859.1:c.527C>T
  hgvsp: ENSP00000404298.1:p.Ala176Val
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+172C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+172C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*769C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.407C>T
  hgvsp: ENSP00000401564.1:p.Ala136Val
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+172C>T
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2633
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9027
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6090
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13454
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27123
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7766
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2512
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 771
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1345
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala176Val
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP

22-20114075-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114075
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114075
    reference: chr 22
allele count: 2
allele frequency: 6.195019204559534e-5
allele num: 32284
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+184G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+184G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1548G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+184G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.419G>A
  hgvsp: ENSP00000401564.1:p.Cys140Tyr
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+184G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*781G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000404298
  ensembl transcript: ENST00000423859
  gene symbol: RANBP1
  hgvsc: ENST00000423859.1:c.539G>A
  hgvsp: ENSP00000404298.1:p.Cys180Tyr
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2505
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5717
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7046
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24695
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18194
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 701
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Cys180Tyr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS

22-20114078-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114078
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114078
    reference: chr 22
allele count: 25
allele frequency: 8.082767539605561e-4
allele num: 30930
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000404298
  ensembl transcript: ENST00000423859
  gene symbol: RANBP1
  hgvsc: ENST00000423859.1:c.542A>T
  hgvsp: ENSP00000404298.1:p.Gln181Leu
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+187A>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+187A>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*784A>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+187A>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1551A>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.422A>T
  hgvsp: ENSP00000401564.1:p.Gln141Leu
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+187A>T
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6489
  bin: 1.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19653
  bin: 2.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23796
  bin: 7.5e0
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2472
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5659
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1446
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 740
  bin: 6.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 760
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gln181Leu
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

22-20114079-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114079
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114079
    reference: chr 22
allele count: 1
allele frequency: 3.271823059808926e-5
allele num: 30564
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.423G>T
  hgvsp: ENSP00000401564.1:p.Gln141His
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000404298
  ensembl transcript: ENST00000423859
  gene symbol: RANBP1
  hgvsc: ENST00000423859.1:c.543G>T
  hgvsp: ENSP00000404298.1:p.Gln181His
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*785G>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1552G>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+188G>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+188G>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+188G>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+188G>T
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2465
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5638
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23514
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6343
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20075
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 469
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 731
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gln181His
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

22-20114080-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114080
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114080
    reference: chr 22
allele count: 3
allele frequency: 9.925229934493483e-5
allele num: 30226
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+189T>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+189T>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000404298
  ensembl transcript: ENST00000423859
  gene symbol: RANBP1
  hgvsc: ENST00000423859.1:c.544T>G
  hgvsp: ENSP00000404298.1:p.Cys182Gly
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*786T>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1553T>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+189T>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.424T>G
  hgvsp: ENSP00000401564.1:p.Cys142Gly
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+189T>G
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6158
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23227
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5627
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20554
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2456
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 457
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 720
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 745
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Cys182Gly
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

22-20114081-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114081
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114081
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 29714
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+190G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+190G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000404298
  ensembl transcript: ENST00000423859
  gene symbol: RANBP1
  hgvsc: ENST00000423859.1:c.545G>A
  hgvsp: ENSP00000404298.1:p.Cys182Tyr
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+190G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1554G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.425G>A
  hgvsp: ENSP00000401564.1:p.Cys142Tyr
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*787G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+190G>A
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5997
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5603
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20942
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22999
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1500
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 731
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 793
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22912
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Cys182Tyr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD

22-20114087-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114087
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114087
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 27188
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+196G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.431G>A
  hgvsp: ENSP00000401564.1:p.Trp144Ter
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+196G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*793G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+196G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1560G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+196G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000404298
  ensembl transcript: ENST00000423859
  gene symbol: RANBP1
  hgvsc: ENST00000423859.1:c.551G>A
  hgvsp: ENSP00000404298.1:p.Trp184Ter
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: stop gained
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 21279
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4948
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23521
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5541
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1495
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7108
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Trp184Ter
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

22-20114090-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114090
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114090
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 26346
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+199C>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.434C>G
  hgvsp: ENSP00000401564.1:p.Pro145Arg
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+199C>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000404298
  ensembl transcript: ENST00000423859
  gene symbol: RANBP1
  hgvsc: ENST00000423859.1:c.554C>G
  hgvsp: ENSP00000404298.1:p.Pro185Arg
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+199C>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1563C>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*796C>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+199C>G
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20367
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24752
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4527
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5521
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 726
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7120
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19628
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro185Arg
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum

22-20114092-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114092
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114092
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 25634
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1565C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000404298
  ensembl transcript: ENST00000423859
  gene symbol: RANBP1
  hgvsc: ENST00000423859.1:c.556C>T
  hgvsp: ENSP00000404298.1:p.Gln186Ter
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+201C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.436C>T
  hgvsp: ENSP00000401564.1:p.Gln146Ter
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*798C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+201C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+201C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+201C>T
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: stop gained
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5505
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25654
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19635
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1383
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1061
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gln186Ter
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

22-20114099-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114099
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114099
    reference: chr 22
allele count: 1
allele frequency: 4.210880916287688e-5
allele num: 23748
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.443A>G
  hgvsp: ENSP00000401564.1:p.Asn148Ser
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+208A>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000404298
  ensembl transcript: ENST00000423859
  gene symbol: RANBP1
  hgvsc: ENST00000423859.1:c.563A>G
  hgvsp: ENSP00000404298.1:p.Asn188Ser
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+208A>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+208A>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*805A>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+208A>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1572A>G
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5454
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16724
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28950
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3326
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2363
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28950
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asn188Ser
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

22-20114119-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114119
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114119
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 19302
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+228C>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1592C>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+228C>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*825C>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+228C>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000404298
  ensembl transcript: ENST00000423859
  gene symbol: RANBP1
  hgvsc: ENST00000423859.1:c.583C>G
  hgvsp: ENSP00000404298.1:p.Arg195Gly
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.463C>G
  hgvsp: ENSP00000401564.1:p.Arg155Gly
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+228C>G
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9487
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34900
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5358
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33841
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1178
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg195Gly
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

22-20114125-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114125
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114125
    reference: chr 22
allele count: 2
allele frequency: 1.077702338614075e-4
allele num: 18558
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1598C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+234C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+234C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*831C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+234C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+234C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000404298
  ensembl transcript: ENST00000423859
  gene symbol: RANBP1
  hgvsc: ENST00000423859.1:c.589C>T
  hgvsp: ENST00000423859.1:c.589C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.469C>T
  hgvsp: ENST00000430524.1:c.469C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7428
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35404
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5320
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33734
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2487
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1247
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5091
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Leu197Leu
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ

22-20114141-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114141
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114141
    reference: chr 22
allele count: 1
allele frequency: 5.640794223826715e-5
allele num: 17728
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*847A>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+250A>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000404298
  ensembl transcript: ENST00000423859
  gene symbol: RANBP1
  hgvsc: ENST00000423859.1:c.605A>T
  hgvsp: ENSP00000404298.1:p.Gln202Leu
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1614A>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+250A>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.485A>T
  hgvsp: ENSP00000401564.1:p.Gln162Leu
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+250A>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+250A>T
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4743
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5276
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2193
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34695
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32753
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 655
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gln202Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: A
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

22-20114152-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114152
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114152
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 17226
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.496T>C
  hgvsp: ENSP00000401564.1:p.Tyr166His
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+261T>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1625T>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*858T>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+261T>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+261T>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+261T>C
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2129
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32557
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5117
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3577
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2909
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2689
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6525
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Tyr166His
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
reference allele: T
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

22-20114164-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114164
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114164
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 16472
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1637C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*870C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.508C>T
  hgvsp: ENSP00000401564.1:p.Arg170Trp
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+273C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+273C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+273C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+273C>T
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29090
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4711
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2721
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1904
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5848
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2210
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 506
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25102
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg170Trp
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD

22-20114170-GTC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114170
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114168
    reference: chr 22
allele count: 1
allele frequency: 6.227425582264292e-5
allele num: 16058
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*881_*882delTC
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1648_1649delTC
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+284_505+285delTC
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+284_505+285delTC
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.519_520delTC
  hgvsp: ENSP00000401564.1:p.Gln174GlufsTer18
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+284_355+285delTC
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+284_286+285delTC
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 4454
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28090
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2680
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3856
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 475
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24383
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2394
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gln174GlufsTer18
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: GTC
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

22-20114176-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114176
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114176
    reference: chr 22
allele count: 1
allele frequency: 6.41025641025641e-5
allele num: 15600
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+285C>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*882C>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+285C>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+285C>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+285C>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1649C>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.520C>G
  hgvsp: ENSP00000401564.1:p.Gln174Glu
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4041
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27191
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 460
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2671
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23478
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gln174Glu
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/22-20114177-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114177
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114177
    reference: chr 22
allele count: 2
allele frequency: 1.287166945552838e-4
allele num: 15538
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.505+286A>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.521A>C
  hgvsp: ENSP00000401564.1:p.Gln174Pro
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*883A>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1650A>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.505+286A>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.355+286A>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.286+286A>C
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2745
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3986
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27032
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 512
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3749
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4898
  bin: 6.25e1
  variant carriers: 1
hgvs: p.Gln174Pro
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

22-20114235-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114235
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114235
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 10410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.*33G>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*941G>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.356-243G>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.287-240G>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.506-243G>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.506-240G>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1708G>C
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2758
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28944
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5073
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1042
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4561
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1018
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 901
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24619
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: Latino
reference allele: G
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

22-20114239-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114239
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114239
    reference: chr 22
allele count: 41
allele frequency: 4.04100137985413e-3
allele num: 10146
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1712T>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.287-236T>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.506-239T>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.*37T>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*945T>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.506-236T>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.356-239T>G
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2627
  bin: 1.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29427
  bin: 2.5e0
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5408
  bin: 7.5e0
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 8.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 748
  bin: 2.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 4595
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 4418
  bin: 2.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 1013
  bin: 1.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 8.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 4.25e1
  variant carriers: 2
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP

22-20114436-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114436
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114436
    reference: chr 22
allele count: 9
allele frequency: 7.467268473192506e-5
allele num: 120526
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.*234C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.506-42C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1909C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.506-39C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.287-39C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.356-42C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*1142C>T
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19209
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25113
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5992
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5531
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2760
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37952
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 818
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

22-20114437-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114437
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114437
    reference: chr 22
allele count: 4
allele frequency: 3.318070210365652e-5
allele num: 120552
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*1143G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.506-38G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.*235G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.356-41G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.506-41G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1910G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.287-38G>A
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25139
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19213
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6050
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5535
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2232
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12508
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 1
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

22-20114448-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114448
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114448
    reference: chr 22
allele count: 1
allele frequency: 8.290911502810618e-6
allele num: 120614
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.506-30T>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.356-30T>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.287-27T>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.506-27T>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.*246T>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*1154T>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1921T>C
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6244
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5531
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19236
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25264
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2762
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

22-20114454-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114454
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114454
    reference: chr 22
allele count: 2
allele frequency: 1.657715005636231e-5
allele num: 120648
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*1160C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.506-21C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.*252C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.287-21C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.356-24C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1927C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.506-24C>T
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25336
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5535
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19258
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6272
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38658
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2757
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2220
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12530
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 345
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

22-20114456-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114456
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114456
    reference: chr 22
allele count: 2
allele frequency: 1.657577616071872e-5
allele num: 120658
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.287-19G>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*1162G>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.*254G>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.506-19G>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.506-22G>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.356-22G>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1929G>T
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5533
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25368
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19256
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6275
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2223
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12541
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38669
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD

22-20114464-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114464
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114463
    reference: chr 22
allele count: 1
allele frequency: 8.282533792737874e-6
allele num: 120736
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.506-13delG
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*1171delG
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.506-10delG
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.*263delG
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.287-10delG
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1938delG
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.356-13delG
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19277
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5530
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6343
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2220
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2757
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 815
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: TG
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum

22-20114468-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114468
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114468
    reference: chr 22
allele count: 1
allele frequency: 8.281436332317477e-6
allele num: 120752
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.506-7T>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1941T>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.*266T>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.356-10T>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*1174T>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.506-10T>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.287-7T>G
  variant of: http://identifiers.org/hgnc/9847
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19279
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5533
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6356
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25430
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38872
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2300
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: c.506-7T>G
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

22-20114472-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114472
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114473
    reference: chr 22
allele count: 1
allele frequency: 8.279653579294243e-6
allele num: 120778
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.506-5dupA
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.*271dupA
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1946dupA
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.356-5dupA
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*1179dupA
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.506-2dupA
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.287-2dupA
  variant of: http://identifiers.org/hgnc/9847
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6373
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25442
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19282
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5530
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 814
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2760
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2224
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
hgvs: c.506-2dupA
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

22-20114474-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114474
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114474
    reference: chr 22
allele count: 1
allele frequency: 8.278556881964336e-6
allele num: 120794
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1947G>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.356-4G>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.*272G>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.506-4G>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.506-1G>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*1180G>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.287-1G>T
  variant of: http://identifiers.org/hgnc/9847
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19285
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6376
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5534
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2227
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38900
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.75e1
  variant carriers: 0
hgvs: c.506-1G>T
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

22-20114478-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114478
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114478
    reference: chr 22
allele count: 1
allele frequency: 8.276501357346223e-6
allele num: 120824
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.290G>A
  hgvsp: ENSP00000398300.1:p.Gly97Glu
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.506G>A
  hgvsp: ENSP00000384925.1:p.Gly169Glu
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.356G>A
  hgvsp: ENSP00000413502.2:p.Gly119Glu
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.*276G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1951G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.509G>A
  hgvsp: ENSP00000327583.3:p.Gly170Glu
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*1184G>A
  variant of: http://identifiers.org/hgnc/9847
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25475
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6395
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5530
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19289
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2225
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gly170Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS

22-20114479-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114479
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114479
    reference: chr 22
allele count: 7
allele frequency: 5.793550950142356e-5
allele num: 120824
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1952A>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*1185A>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.291A>G
  hgvsp: ENST00000448394.1:c.291A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.510A>G
  hgvsp: ENST00000331821.3:c.510A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.357A>G
  hgvsp: ENST00000418705.2:c.357A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.507A>G
  hgvsp: ENST00000402752.1:c.507A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.*277A>G
  variant of: http://identifiers.org/hgnc/9847
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19289
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6393
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5531
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25480
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12571
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 815
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2761
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2298
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
hgvs: c.507A>G
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

22-20114486-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114486
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114486
    reference: chr 22
allele count: 1
allele frequency: 8.273351534706709e-6
allele num: 120870
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.298A>G
  hgvsp: ENSP00000398300.1:p.Lys100Glu
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.517A>G
  hgvsp: ENSP00000327583.3:p.Lys173Glu
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.514A>G
  hgvsp: ENSP00000384925.1:p.Lys172Glu
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.364A>G
  hgvsp: ENSP00000413502.2:p.Lys122Glu
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.*284A>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*1192A>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1959A>G
  variant of: http://identifiers.org/hgnc/9847
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25496
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5533
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6411
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19296
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12575
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 812
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39010
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Lys173Glu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

22-20114490-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114490
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114490
    reference: chr 22
allele count: 1
allele frequency: 8.271982794275789e-6
allele num: 120890
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.368A>G
  hgvsp: ENSP00000413502.2:p.Asn123Ser
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.521A>G
  hgvsp: ENSP00000327583.3:p.Asn174Ser
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.*288A>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1963A>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*1196A>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.518A>G
  hgvsp: ENSP00000384925.1:p.Asn173Ser
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.302A>G
  hgvsp: ENSP00000398300.1:p.Asn101Ser
  variant of: http://identifiers.org/hgnc/9847
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6420
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19294
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5532
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25501
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 812
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39026
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2758
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asn174Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

22-20114500-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114500
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114500
    reference: chr 22
allele count: 1
allele frequency: 8.270888127967181e-6
allele num: 120906
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.531C>G
  hgvsp: ENST00000331821.3:c.531C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1973C>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.528C>G
  hgvsp: ENST00000402752.1:c.528C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.378C>G
  hgvsp: ENST00000418705.2:c.378C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*1206C>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.312C>G
  hgvsp: ENST00000448394.1:c.312C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.*298C>G
  variant of: http://identifiers.org/hgnc/9847
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6434
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5533
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25504
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19296
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2292
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 811
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ala177Ala
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

22-20114500-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114500
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114500
    reference: chr 22
allele count: 5
allele frequency: 4.13544406398359e-5
allele num: 120906
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.528C>T
  hgvsp: ENST00000402752.1:c.528C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*1206C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.312C>T
  hgvsp: ENST00000448394.1:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.378C>T
  hgvsp: ENST00000418705.2:c.378C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.*298C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.531C>T
  hgvsp: ENST00000331821.3:c.531C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1973C>T
  variant of: http://identifiers.org/hgnc/9847
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6434
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25504
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5533
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19296
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2224
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2754
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 811
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala177Ala
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: African
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ

22-20114502-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114502
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114502
    reference: chr 22
allele count: 1
allele frequency: 8.269656974628692e-6
allele num: 120924
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.*300A>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.380A>G
  hgvsp: ENSP00000413502.2:p.Glu127Gly
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.533A>G
  hgvsp: ENSP00000327583.3:p.Glu178Gly
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1975A>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.314A>G
  hgvsp: ENSP00000398300.1:p.Glu105Gly
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.530A>G
  hgvsp: ENSP00000384925.1:p.Glu177Gly
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*1208A>G
  variant of: http://identifiers.org/hgnc/9847
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25512
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19297
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6434
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5532
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39062
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 811
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Glu178Gly
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

22-20114511-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114511
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114511
    reference: chr 22
allele count: 5
allele frequency: 4.134896875671921e-5
allele num: 120922
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.539C>T
  hgvsp: ENSP00000384925.1:p.Ala180Val
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.323C>T
  hgvsp: ENSP00000398300.1:p.Ala108Val
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.389C>T
  hgvsp: ENSP00000413502.2:p.Ala130Val
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*1217C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.542C>T
  hgvsp: ENSP00000327583.3:p.Ala181Val
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1984C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.*309C>T
  variant of: http://identifiers.org/hgnc/9847
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19295
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5533
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6428
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25512
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2225
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 811
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala181Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

22-20114512-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114512
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114512
    reference: chr 22
allele count: 398
allele frequency: 3.291432351968244e-3
allele num: 120920
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*1218G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.324G>A
  hgvsp: ENST00000448394.1:c.324G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.543G>A
  hgvsp: ENST00000331821.3:c.543G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.540G>A
  hgvsp: ENST00000402752.1:c.540G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1985G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.390G>A
  hgvsp: ENST00000418705.2:c.390G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.*310G>A
  variant of: http://identifiers.org/hgnc/9847
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25506
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 19269
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6405
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5495
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 4.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.75e1
  variant carriers: 180
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 23
genotype quality: GenotypeQuality
  all individuals: 800
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala181Ala
num of homozygotes: 5
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

22-20114512-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114512
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114512
    reference: chr 22
allele count: 2
allele frequency: 1.653986106516705e-5
allele num: 120920
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*1218G>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1985G>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.*310G>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.543G>T
  hgvsp: ENST00000331821.3:c.543G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.540G>T
  hgvsp: ENST00000402752.1:c.540G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.390G>T
  hgvsp: ENST00000418705.2:c.390G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.324G>T
  hgvsp: ENST00000448394.1:c.324G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19269
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 25506
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5495
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6405
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2214
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2740
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2364
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala181Ala
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

22-20114518-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114518
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114518
    reference: chr 22
allele count: 225
allele frequency: 1.860672819291456e-3
allele num: 120924
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.396G>A
  hgvsp: ENST00000418705.2:c.396G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.*316G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.549G>A
  hgvsp: ENST00000331821.3:c.549G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.330G>A
  hgvsp: ENST00000448394.1:c.330G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*1224G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.1991G>A
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.546G>A
  hgvsp: ENST00000402752.1:c.546G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 5514
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6402
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 19378
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 25637
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 9.75e1
  variant carriers: 82
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.25e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12640
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39261
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Lys183Lys
num of homozygotes: 4
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum

22-20114527-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114527
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114527
    reference: chr 22
allele count: 2
allele frequency: 1.654150263009892e-5
allele num: 120908
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.555T>G
  hgvsp: ENST00000402752.1:c.555T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.339T>G
  hgvsp: ENST00000448394.1:c.339T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.558T>G
  hgvsp: ENST00000331821.3:c.558T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.405T>G
  hgvsp: ENST00000418705.2:c.405T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*1233T>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.*325T>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.2000T>G
  variant of: http://identifiers.org/hgnc/9847
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5533
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6380
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19444
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25731
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2758
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala186Ala
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

22-20114532-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114532
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114532
    reference: chr 22
allele count: 3
allele frequency: 2.481553783542335e-5
allele num: 120892
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.*330C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.563C>T
  hgvsp: ENSP00000327583.3:p.Ser188Leu
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.2005C>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.410C>T
  hgvsp: ENSP00000413502.2:p.Ser137Leu
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.560C>T
  hgvsp: ENSP00000384925.1:p.Ser187Leu
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.344C>T
  hgvsp: ENSP00000398300.1:p.Ser115Leu
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*1238C>T
  variant of: http://identifiers.org/hgnc/9847
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19440
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6354
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5534
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25733
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 802
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2214
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ser188Leu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: African
population: South Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

22-20114537-AAGG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114537
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114534
    reference: chr 22
allele count: 1
allele frequency: 8.273351534706709e-6
allele num: 120870
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.2016_2018delGAG
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*1249_*1251delGAG
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.*341_*343delGAG
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.355_357delGAG
  hgvsp: ENSP00000398300.1:p.Glu119del
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.574_576delGAG
  hgvsp: ENSP00000327583.3:p.Glu192del
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.421_423delGAG
  hgvsp: ENSP00000413502.2:p.Glu141del
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.571_573delGAG
  hgvsp: ENSP00000384925.1:p.Glu191del
  variant of: http://identifiers.org/hgnc/9847
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5532
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19439
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6339
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25742
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2208
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12689
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39333
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Glu192del
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: AAGG
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

http://identifiers.org/exac.variant/22-20114541-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114541
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114541
    reference: chr 22
allele count: 1
allele frequency: 8.276501357346223e-6
allele num: 120824
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.2014A>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.*339A>C
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.353A>C
  hgvsp: ENSP00000398300.1:p.Glu118Ala
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.572A>C
  hgvsp: ENSP00000327583.3:p.Glu191Ala
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.569A>C
  hgvsp: ENSP00000384925.1:p.Glu190Ala
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.419A>C
  hgvsp: ENSP00000413502.2:p.Glu140Ala
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*1247A>C
  variant of: http://identifiers.org/hgnc/9847
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25728
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19436
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5531
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6295
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2205
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2749
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39261
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1864
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu191Ala
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

22-20114550-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114550
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114550
    reference: chr 22
allele count: 3
allele frequency: 2.484184028352821e-5
allele num: 120764
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*1256A>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.578A>G
  hgvsp: ENSP00000384925.1:p.Lys193Arg
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.581A>G
  hgvsp: ENSP00000327583.3:p.Lys194Arg
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.362A>G
  hgvsp: ENSP00000398300.1:p.Lys121Arg
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.428A>G
  hgvsp: ENSP00000413502.2:p.Lys143Arg
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.2023A>G
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.*348A>G
  variant of: http://identifiers.org/hgnc/9847
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19424
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5529
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25726
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1862
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2199
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2745
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 416
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Lys194Arg
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum

22-20114554-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 20114554
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 20114554
    reference: chr 22
allele count: 1
allele frequency: 8.286239870071759e-6
allele num: 120682
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000413502
  ensembl transcript: ENST00000418705
  gene symbol: RANBP1
  hgvsc: ENST00000418705.2:c.432G>T
  hgvsp: ENSP00000413502.2:p.Glu144Asp
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000327583
  ensembl transcript: ENST00000331821
  gene symbol: RANBP1
  hgvsc: ENST00000331821.3:c.585G>T
  hgvsp: ENSP00000327583.3:p.Glu195Asp
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000398300
  ensembl transcript: ENST00000448394
  gene symbol: RANBP1
  hgvsc: ENST00000448394.1:c.366G>T
  hgvsp: ENSP00000398300.1:p.Glu122Asp
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000401564
  ensembl transcript: ENST00000430524
  gene symbol: RANBP1
  hgvsc: ENST00000430524.1:c.*352G>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099901
  ensembl transcript: ENST00000486575
  gene symbol: RANBP1
  hgvsc: ENST00000486575.1:n.2027G>T
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000384925
  ensembl transcript: ENST00000402752
  gene symbol: RANBP1
  hgvsc: ENST00000402752.1:c.582G>T
  hgvsp: ENSP00000384925.1:p.Glu194Asp
  variant of: http://identifiers.org/hgnc/9847
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099901
  ensembl protein: ENSP00000390139
  ensembl transcript: ENST00000435265
  gene symbol: RANBP1
  hgvsc: ENST00000435265.1:c.*1260G>T
  variant of: http://identifiers.org/hgnc/9847
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6192
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5522
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19415
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25698
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2199
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39130
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 328
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Glu195Asp
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 314
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6768
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1526
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 628
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45244
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 343
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1594
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9982
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16134
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64962
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8434
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.857395925597875e-5
allele num: 11290
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6540
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.705e0

DP
type: SiteQuality
SIO_000300: 1.53731e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.37e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 7.27e0

VQSLOD
type: SiteQuality
SIO_000300: 6.7e-2

GenotypeQuality
all individuals: 222
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3429
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1501
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 43920
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 562
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1421
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15968
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.558360604643914e-5
allele num: 64170
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11172
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8316
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9842
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6494
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.84e-1

QD
type: SiteQuality
SIO_000300: 1.64e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

MQ
type: SiteQuality
SIO_000300: 5.962e1

MQRankSum
type: SiteQuality
SIO_000300: 5.79e-1

DP
type: SiteQuality
SIO_000300: 1.50887e6

FS
type: SiteQuality
SIO_000300: 6.954e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.370000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.357e0

VQSLOD
type: SiteQuality
SIO_000300: -1.683e0

GenotypeQuality
all individuals: 57
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 262
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 746
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5978
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10976
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6428
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8188
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9756
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.158459934935725e-5
allele num: 63322
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15810
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.468e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

DP
type: SiteQuality
SIO_000300: 1.475222e6

MQRankSum
type: SiteQuality
SIO_000300: 1.32e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.29e-1

FS
type: SiteQuality
SIO_000300: 1.3416e1

QD
type: SiteQuality
SIO_000300: 1.01e1

VQSLOD
type: SiteQuality
SIO_000300: -1.936e0

MQ
type: SiteQuality
SIO_000300: 5.881e1

GenotypeQuality
all individuals: 37
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1234
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 424
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variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62342
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9632
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.39467962655071e-5
allele num: 15638
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.239157372986369e-4
allele num: 8070
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10762
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6354
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -3.18e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.34e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.86e0

DP
type: SiteQuality
SIO_000300: 1.438328e6

QD
type: SiteQuality
SIO_000300: 1.261e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.78e0

FS
type: SiteQuality
SIO_000300: 4.043e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.68e-1

GenotypeQuality
all individuals: 5653
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 422
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 657
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 399
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GenotypeQuality
all individuals: 119
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9608
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15612
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6336
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.609217598403656e-5
allele num: 62142
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8048
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 2.262e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.209e0

MQRankSum
type: SiteQuality
SIO_000300: 6.919999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.600000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.919999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.72e-1

QD
type: SiteQuality
SIO_000300: 1.334e1

DP
type: SiteQuality
SIO_000300: 1.431142e6

GenotypeQuality
all individuals: 3965
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 655
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 131
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GenotypeQuality
all individuals: 785
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.1059500110595e-4
allele num: 9042
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7522
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9842
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57642
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14912
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5970
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.7e0

DP
type: SiteQuality
SIO_000300: 1.286019e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.278e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.79e-1

QD
type: SiteQuality
SIO_000300: 1.496e1

FS
type: SiteQuality
SIO_000300: 9.634e0

MQRankSum
type: SiteQuality
SIO_000300: -5.13e-1

MQ
type: SiteQuality
SIO_000300: 5.899e1

GenotypeQuality
all individuals: 810
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 794
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.894649751792609e-5
allele num: 14504
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7220
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54770
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9206
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 772
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5738
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.8e-1

DP
type: SiteQuality
SIO_000300: 1.194769e6

BaseQRankSum
type: SiteQuality
SIO_000300: 6.08e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 8.53e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.52e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.32e-1

QD
type: SiteQuality
SIO_000300: 1.328e1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 6

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6942
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.221001221001221e-4
allele num: 8190
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8680
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14160
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 758
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 9.626121443148127e-5
allele num: 51942
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.04e0

VQSLOD
type: SiteQuality
SIO_000300: 3.62e0

MQ
type: SiteQuality
SIO_000300: 5.892e1

DP
type: SiteQuality
SIO_000300: 1.11212e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.01e0

QD
type: SiteQuality
SIO_000300: 1.309e1

MQRankSum
type: SiteQuality
SIO_000300: -3.87e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.11e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2068
bin: 3.75e1
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GenotypeQuality
all individuals: 23403
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5508
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 4.884004884004884e-4
allele num: 8190
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14160
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6942
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51942
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8680
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 758
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

MQ
type: SiteQuality
SIO_000300: 5.892e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.01e0

FS
type: SiteQuality
SIO_000300: 1.04e0

MQRankSum
type: SiteQuality
SIO_000300: -3.87e-1

DP
type: SiteQuality
SIO_000300: 1.11212e6

QD
type: SiteQuality
SIO_000300: 1.309e1

VQSLOD
type: SiteQuality
SIO_000300: 3.62e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.63e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.11e-1

GenotypeQuality
all individuals: 573
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 124
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GenotypeQuality
all individuals: 468
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GenotypeQuality
all individuals: 518
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GenotypeQuality
all individuals: 206
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GenotypeQuality
all individuals: 2735
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GenotypeQuality
all individuals: 3054
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GenotypeQuality
all individuals: 68
bin: 8.75e1
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GenotypeQuality
all individuals: 2102
bin: 3.75e1
variant carriers: 0

Latino
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allele count: 0
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Other
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European (Non-Finnish)
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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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FS
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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QD
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DP
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Non-Finnish)
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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Other
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FS
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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DP
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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African
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European (Non-Finnish)
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Other
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Latino
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ClippingRankSum
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MQ
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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FS
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MQRankSum
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DP
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QD
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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East Asian
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European (Non-Finnish)
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Latino
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Other
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FS
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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DP
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VQSLOD
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MQRankSum
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MQ
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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East Asian
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European (Non-Finnish)
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European (Finnish)
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South Asian
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ClippingRankSum
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MQRankSum
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DP
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FS
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QD
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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Other
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European (Finnish)
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Latino
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European (Non-Finnish)
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South Asian
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MQ
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BaseQRankSum
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DP
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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FS
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InbreedingCoeff
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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African
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Latino
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European (Finnish)
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Other
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South Asian
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VQSLOD
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FS
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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DP
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MQ
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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South Asian
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African
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Latino
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FS
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MQRankSum
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MQ
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DP
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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South Asian
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Latino
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East Asian
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African
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European (Finnish)
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MQ
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DP
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FS
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: -7.900000000000001e-3

QD
type: SiteQuality
SIO_000300: 1.063e1

VQSLOD
type: SiteQuality
SIO_000300: -1.273e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.72e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.74e-1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 523
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variant carriers: 0

GenotypeQuality
all individuals: 3021
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4124
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5948
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 612
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5072
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11992
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5844
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.771157789724547e-5
allele num: 36086
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.409e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.239e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.239e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.18e0

MQRankSum
type: SiteQuality
SIO_000300: -1.468e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.9e-3

DP
type: SiteQuality
SIO_000300: 8.0961e5

QD
type: SiteQuality
SIO_000300: 3.56e0

GenotypeQuality
all individuals: 291
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3932
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4770
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 576
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11638
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.930494603249911e-5
allele num: 33724
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5482
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5534
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.52e-1

FS
type: SiteQuality
SIO_000300: 4.873e0

QD
type: SiteQuality
SIO_000300: 1.509e1

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.85e0

DP
type: SiteQuality
SIO_000300: 7.8334e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.01e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.76e0

VQSLOD
type: SiteQuality
SIO_000300: 2.28e-1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4684
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 1.507658907248824e-4
allele num: 33164
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3874
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5412
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5408
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 570
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.1e-2

DP
type: SiteQuality
SIO_000300: 7.80152e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.08e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.71e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.95e-1

FS
type: SiteQuality
SIO_000300: 2.957e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.56e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 154
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5144
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.160955873056012e-5
allele num: 31636
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.763357432551578e-4
allele num: 11342
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5082
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4494
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.668089647812167e-4
allele num: 3748
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 550
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.61255e5

FS
type: SiteQuality
SIO_000300: 4.014e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.83e-1

MQ
type: SiteQuality
SIO_000300: 5.894e1

MQRankSum
type: SiteQuality
SIO_000300: -3.5e-2

QD
type: SiteQuality
SIO_000300: 1.379e1

VQSLOD
type: SiteQuality
SIO_000300: -1.723e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.12e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.73e-1

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 2.004811547714515e-4
allele num: 4988
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.718868950516585e-4
allele num: 3678
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 542
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5036
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11238
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 6.433350488934638e-5
allele num: 31088
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4428
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.179999999999999e-1

DP
type: SiteQuality
SIO_000300: 7.54178e5

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.07e-2

QD
type: SiteQuality
SIO_000300: 1.317e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.94e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.5e0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5036
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3678
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11238
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 6.433350488934638e-5
allele num: 31088
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 4428
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 542
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African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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VQSLOD
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ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 7.54178e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.07e-2

QD
type: SiteQuality
SIO_000300: 1.317e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3350
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 476
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 3900
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10724
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4260
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4378
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 3.664883090229422e-5
allele num: 27286
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.978e0

InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 8.48e-1

QD
type: SiteQuality
SIO_000300: 1.945e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.7e-2

DP
type: SiteQuality
SIO_000300: 7.05221e5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 49
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2720
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 17246
num of homozygotes: 0

East Asian
type: Population
allele count: 6
allele frequency: 2.597402597402597e-3
allele num: 2310
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.072501072501073e-4
allele num: 9324
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 2706
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2470
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 354
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.377e0

MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.96e-2

DP
type: SiteQuality
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2296
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 1.381406271584473e-4
allele num: 14478
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 2112
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2296
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 320
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 1838
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.09e0

DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.69e-2

VQSLOD
type: SiteQuality
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MQRankSum
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SIO_000300: -3.11e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
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FS
type: SiteQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 34

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 1720
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8816
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 310
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European (Finnish)
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allele count: 2
allele frequency: 8.960573476702509e-4
allele num: 2232
num of homozygotes: 0

European (Non-Finnish)
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allele count: 23
allele frequency: 1.678587067581375e-3
allele num: 13702
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 1950
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 2200
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ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
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SIO_000300: 5.23633e5

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
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BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 6.23e-1

InbreedingCoeff
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SIO_000300: -3.87e-2

MQ
type: SiteQuality
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 1904
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 2180
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South Asian
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allele count: 1
allele frequency: 1.134816159782115e-4
allele num: 8812
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2214
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 1682
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 13464
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.47e-1

FS
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ClippingRankSum
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BaseQRankSum
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DP
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ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 5.968e1

VQSLOD
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.02e-2

QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8768
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 3
allele frequency: 1.607717041800643e-3
allele num: 1866
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 1640
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2198
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 13290
num of homozygotes: 0

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.098e0

MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 5.15575e5

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.51e-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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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8736
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2198
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 296
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12976
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 2118
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 1592
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 1798
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.47e-1

DP
type: SiteQuality
SIO_000300: 5.12132e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.16e-2

MQ
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
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MQRankSum
type: SiteQuality
SIO_000300: -7.47e-1

FS
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ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
allele num: 8546
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 272
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 1934
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

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

InbreedingCoeff
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VQSLOD
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FS
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ClippingRankSum
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BaseQRankSum
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MQ
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QD
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DP
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MQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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European (Finnish)
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Latino
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African
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South Asian
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QD
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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DP
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MQ
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ReadPosRankSum
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FS
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6.75e1
variant carriers: 0

European (Finnish)
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allele frequency: 0.0e0
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South Asian
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Other
type: Population
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Latino
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African
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East Asian
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European (Non-Finnish)
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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MQ
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FS
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MQRankSum
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ClippingRankSum
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DP
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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East Asian
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European (Non-Finnish)
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European (Finnish)
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Other
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African
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South Asian
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InbreedingCoeff
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MQ
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FS
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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VQSLOD
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6885
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1252
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 658
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7036
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 230
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7914
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1694
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 518
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.71685e5

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.94e0

VQSLOD
type: SiteQuality
SIO_000300: -1.608e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.34e-2

FS
type: SiteQuality
SIO_000300: 8.073e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.93e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.92e0

QD
type: SiteQuality
SIO_000300: 1.285e1

GenotypeQuality
all individuals: 45
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6830
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 224
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1206
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.549719530851606e-4
allele num: 7844
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1640
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 452
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 608
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.41e-1

DP
type: SiteQuality
SIO_000300: 3.51503e5

BaseQRankSum
type: SiteQuality
SIO_000300: -3.187e0

QD
type: SiteQuality
SIO_000300: 1.289e1

MQRankSum
type: SiteQuality
SIO_000300: -3.6e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.530000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.9e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.225e-1

FS
type: SiteQuality
SIO_000300: 3.818e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

GenotypeQuality
all individuals: 39
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 46
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6090
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1572
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 4.761904761904762e-3
allele num: 210
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 380
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1146
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 570
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7760
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.262e1

FS
type: SiteQuality
SIO_000300: 2.255e0

DP
type: SiteQuality
SIO_000300: 3.21616e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.698e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e0

MQRankSum
type: SiteQuality
SIO_000300: -1.145e0

VQSLOD
type: SiteQuality
SIO_000300: -3.333e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.93e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.874e0

MQ
type: SiteQuality
SIO_000300: 5.975e1

GenotypeQuality
all individuals: 182
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30131
bin: 7.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 40
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GenotypeQuality
all individuals: 42
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1104
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 362
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7690
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5850
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1470
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 552
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 3.01197e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -7.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.06e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.2e-1

QD
type: SiteQuality
SIO_000300: 8.140000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.2e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.352e0

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 417
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4203
bin: 2.5e0
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
all individuals: 580
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 9.75e1
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GenotypeQuality
all individuals: 166
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 544
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1064
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 342
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7456
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5560
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 194
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1312
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.28e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.21e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.97e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

DP
type: SiteQuality
SIO_000300: 2.72801e5

FS
type: SiteQuality
SIO_000300: 4.692e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.21e-1

MQ
type: SiteQuality
SIO_000300: 5.705e1

MQRankSum
type: SiteQuality
SIO_000300: 9.56e-1

QD
type: SiteQuality
SIO_000300: 1.276e1

GenotypeQuality
all individuals: 377
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
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variant carriers: 0

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

GenotypeQuality
all individuals: 5450
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 561
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variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 9.75e1
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GenotypeQuality
all individuals: 201
bin: 2.75e1
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GenotypeQuality
all individuals: 210
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7298
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 336
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1248
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 544
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1054
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.855287569573284e-4
allele num: 5390
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.63e-1

QD
type: SiteQuality
SIO_000300: 1.822e1

VQSLOD
type: SiteQuality
SIO_000300: -1.05e0

MQ
type: SiteQuality
SIO_000300: 6.153e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.19e-2

FS
type: SiteQuality
SIO_000300: 2.451e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.355e0

DP
type: SiteQuality
SIO_000300: 2.62533e5

GenotypeQuality
all individuals: 130
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3834
bin: 2.5e0
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GenotypeQuality
all individuals: 86
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 69
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GenotypeQuality
all individuals: 4990
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 147
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GenotypeQuality
all individuals: 42
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7054
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1064
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 182
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1174
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.905487804878049e-4
allele num: 5248
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 336
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.13e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.1e-2

MQ
type: SiteQuality
SIO_000300: 5.801e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.04e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.52776e5

VQSLOD
type: SiteQuality
SIO_000300: -1.785e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.27e0

QD
type: SiteQuality
SIO_000300: 7.3e0

GenotypeQuality
all individuals: 51
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2746
bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 23372
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1064
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 182
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1168
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 336
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5230
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 542
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.850627137970354e-4
allele num: 7016
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.50381e5

QD
type: SiteQuality
SIO_000300: 9.93e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.09e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.289e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.57e-1

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.93e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 721
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variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 488
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 686
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3868
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 996
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 114
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3954
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 304
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.91051e5

QD
type: SiteQuality
SIO_000300: 7.71e0

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.58e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.44e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.06e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

GenotypeQuality
all individuals: 44
bin: 9.25e1
variant carriers: 5

GenotypeQuality
all individuals: 152
bin: 9.75e1
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GenotypeQuality
all individuals: 55
bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 327
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GenotypeQuality
all individuals: 125
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variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 490
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 2.127659574468085e-3
allele num: 3760
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 112
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 2.976190476190476e-3
allele num: 672
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 3.311258278145695e-3
allele num: 302
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.01010101010101e-3
allele num: 990
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 29
allele frequency: 7.591623036649215e-3
allele num: 3820
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.77e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.04e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.26e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.210000000000001e-2

QD
type: SiteQuality
SIO_000300: 1.489e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

DP
type: SiteQuality
SIO_000300: 1.92379e5

GenotypeQuality
all individuals: 42
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
all individuals: 287
bin: 8.75e1
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GenotypeQuality
all individuals: 16
bin: 2.5e0
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GenotypeQuality
all individuals: 12489
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2315
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 2227
bin: 7.75e1
variant carriers: 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: 1
allele frequency: 6.069434328720563e-5
allele num: 16476
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.058035984733749e-5
allele num: 66028
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 3.877471888328809e-4
allele num: 10316
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.891e1

VQSLOD
type: SiteQuality
SIO_000300: 9.63e-1

QD
type: SiteQuality
SIO_000300: 1.219e1

FS
type: SiteQuality
SIO_000300: 7.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.4e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.0e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

DP
type: SiteQuality
SIO_000300: 1.853243e6

GenotypeQuality
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2307
bin: 9.75e1
variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 285
bin: 8.75e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 38105
bin: 6.25e1
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GenotypeQuality
all individuals: 2764
bin: 7.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.212709192335678e-4
allele num: 16492
num of homozygotes: 1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66038
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.314814814814815e-4
allele num: 8640
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: 898
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-3

DP
type: SiteQuality
SIO_000300: 1.853365e6

MQ
type: SiteQuality
SIO_000300: 5.928e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.78e-1

QD
type: SiteQuality
SIO_000300: 1.516e1

FS
type: SiteQuality
SIO_000300: 1.705e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.21e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.94e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.69e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.56e0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 38540
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2225
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 12527
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variant carriers: 0

GenotypeQuality
all individuals: 816
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2304
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: 898
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66082
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.680542110358181e-5
allele num: 10330
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.97e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.2e-2

QD
type: SiteQuality
SIO_000300: 1.127e1

DP
type: SiteQuality
SIO_000300: 1.8566e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.53e-1

FS
type: SiteQuality
SIO_000300: 4.128e0

MQ
type: SiteQuality
SIO_000300: 5.884e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.42e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -8.014e-1

GenotypeQuality
all individuals: 2303
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 814
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 318
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variant carriers: 0

GenotypeQuality
all individuals: 17
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 109
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variant carriers: 0

GenotypeQuality
all individuals: 36
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variant carriers: 0

GenotypeQuality
all individuals: 283
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variant carriers: 0

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

African
type: Population
allele count: 2
allele frequency: 1.935359009096187e-4
allele num: 10334
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.3481e1

DP
type: SiteQuality
SIO_000300: 1.858355e6

MQRankSum
type: SiteQuality
SIO_000300: 6.6e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.066e0

QD
type: SiteQuality
SIO_000300: 1.41e1

MQ
type: SiteQuality
SIO_000300: 5.797e1

VQSLOD
type: SiteQuality
SIO_000300: -9.241e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.6e-2

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 815
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2303
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2759
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 2.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66110
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.934984520123839e-4
allele num: 10336
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
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: 7.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 1.6947e1

QD
type: SiteQuality
SIO_000300: 1.353e1

DP
type: SiteQuality
SIO_000300: 1.858696e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.096e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.82e-1

MQ
type: SiteQuality
SIO_000300: 5.799e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.82e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.526e0

GenotypeQuality
all individuals: 38836
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
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variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 290
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variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2302
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 345
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variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12561
bin: 6.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66162
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.182e0

MQ
type: SiteQuality
SIO_000300: 6.098e1

VQSLOD
type: SiteQuality
SIO_000300: 1.39e0

DP
type: SiteQuality
SIO_000300: 1.860323e6

MQRankSum
type: SiteQuality
SIO_000300: 1.56e0

FS
type: SiteQuality
SIO_000300: 1.023e0

QD
type: SiteQuality
SIO_000300: 1.695e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.5e-1

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

GenotypeQuality
all individuals: 2759
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 814
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variant carriers: 0

GenotypeQuality
all individuals: 283
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variant carriers: 0

GenotypeQuality
all individuals: 2222
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variant carriers: 0

GenotypeQuality
all individuals: 345
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variant carriers: 0

GenotypeQuality
all individuals: 12560
bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511121856866538e-5
allele num: 66176
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
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: 902
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.73e-1

MQ
type: SiteQuality
SIO_000300: 5.771e1

MQRankSum
type: SiteQuality
SIO_000300: 5.86e-1

DP
type: SiteQuality
SIO_000300: 1.860858e6

VQSLOD
type: SiteQuality
SIO_000300: -5.929e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.96e-1

QD
type: SiteQuality
SIO_000300: 1.268e1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2300
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10358
num of homozygotes: 0

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

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

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

QD
type: SiteQuality
SIO_000300: 9.74e0

MQRankSum
type: SiteQuality
SIO_000300: 8.28e-1

FS
type: SiteQuality
SIO_000300: 5.216e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.85e-1

DP
type: SiteQuality
SIO_000300: 1.861263e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.139999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.71e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 6.006e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.94e-1

GenotypeQuality
all individuals: 263
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 814
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.75e1
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GenotypeQuality
all individuals: 283
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
all individuals: 2299
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.652015919709292e-5
allele num: 11558
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.924e1

QD
type: SiteQuality
SIO_000300: 1.108e1

FS
type: SiteQuality
SIO_000300: 7.302e0

VQSLOD
type: SiteQuality
SIO_000300: -1.43e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.32e-1

DP
type: SiteQuality
SIO_000300: 1.861564e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.872e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

GenotypeQuality
all individuals: 283
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
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GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 48
bin: 3.25e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
all individuals: 814
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 38961
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2760
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66238
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.106194690265487e-3
allele num: 904
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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.944e0

VQSLOD
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ReadPosRankSum
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SIO_000300: 1.88e0

MQ
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -1.567e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.7e0

DP
type: SiteQuality
SIO_000300: 1.862098e6

FS
type: SiteQuality
SIO_000300: 1.569e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2224
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variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

East Asian
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allele count: 7
allele frequency: 8.101851851851852e-4
allele num: 8640
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66238
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.205e0

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 9.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.896e1

DP
type: SiteQuality
SIO_000300: 1.862383e6

MQRankSum
type: SiteQuality
SIO_000300: 2.6e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.05e0

QD
type: SiteQuality
SIO_000300: 1.3e1

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

DP
type: SiteQuality
SIO_000300: 1.86257e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.58e-1

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 7.18e-1

InbreedingCoeff
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SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.196e1

VQSLOD
type: SiteQuality
SIO_000300: 1.19e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.77e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508477644361311e-5
allele num: 66292
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.922e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.53e-1

DP
type: SiteQuality
SIO_000300: 1.862671e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.1e-2

FS
type: SiteQuality
SIO_000300: 6.973e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.5e0

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

QD
type: SiteQuality
SIO_000300: 1.322e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 12575
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.652015919709292e-5
allele num: 11558
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66308
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 1.863256e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

QD
type: SiteQuality
SIO_000300: 1.242e1

MQRankSum
type: SiteQuality
SIO_000300: 6.75e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.43e0

MQ
type: SiteQuality
SIO_000300: 5.935e1

FS
type: SiteQuality
SIO_000300: 1.103e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.51e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.3e-2

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 245
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GenotypeQuality
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GenotypeQuality
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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: 2292
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GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 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: 1
allele frequency: 1.157407407407407e-4
allele num: 8640
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.524340954334319e-5
allele num: 66308
num of homozygotes: 0

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 6.75e-1

DP
type: SiteQuality
SIO_000300: 1.863256e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.49e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.43e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.3e-2

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.103e0

QD
type: SiteQuality
SIO_000300: 1.242e1

MQ
type: SiteQuality
SIO_000300: 5.935e1

GenotypeQuality
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
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: 0
allele frequency: 0.0e0
allele num: 66322
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 1
allele frequency: 1.157407407407407e-4
allele num: 8640
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

MQRankSum
type: SiteQuality
SIO_000300: 1.47e0

FS
type: SiteQuality
SIO_000300: 1.25e0

DP
type: SiteQuality
SIO_000300: 1.862954e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.14e-1

BaseQRankSum
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VQSLOD
type: SiteQuality
SIO_000300: -7.579e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

QD
type: SiteQuality
SIO_000300: 1.534e1

MQ
type: SiteQuality
SIO_000300: 5.893e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

African
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allele count: 0
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allele num: 10368
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
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European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.015408738654524e-5
allele num: 66326
num of homozygotes: 0

Latino
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allele count: 3
allele frequency: 2.595155709342561e-4
allele num: 11560
num of homozygotes: 0

South Asian
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Other
type: Population
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East Asian
type: Population
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allele num: 8640
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FS
type: SiteQuality
SIO_000300: 5.54e-1

BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.919e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.0e-3

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
allele count: 4
allele frequency: 4.415011037527594e-3
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 263
allele frequency: 3.9652624913307e-3
allele num: 66326
num of homozygotes: 1

African
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allele count: 7
allele frequency: 6.75414897722887e-4
allele num: 10364
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South Asian
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allele frequency: 3.028834504482675e-4
allele num: 16508
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European (Finnish)
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allele count: 111
allele frequency: 1.678258240096765e-2
allele num: 6614
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East Asian
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allele count: 1
allele frequency: 1.157407407407407e-4
allele num: 8640
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Latino
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allele frequency: 6.054315862307559e-4
allele num: 11562
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.881273e6

MQRankSum
type: SiteQuality
SIO_000300: -3.72e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.16e-1

MQ
type: SiteQuality
SIO_000300: 5.757e1

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.218e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 800
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GenotypeQuality
all individuals: 332
bin: 9.25e1
variant carriers: 0

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

African
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allele frequency: 0.0e0
allele num: 10364
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66326
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Other
type: Population
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South Asian
type: Population
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allele frequency: 1.21153380179307e-4
allele num: 16508
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.757e1

FS
type: SiteQuality
SIO_000300: 5.39e-1

BaseQRankSum
type: SiteQuality
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MQRankSum
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.25e-2

QD
type: SiteQuality
SIO_000300: 1.218e1

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2750
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 263
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 798
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2084
bin: 9.75e1
variant carriers: 220

GenotypeQuality
all individuals: 2210
bin: 7.75e1
variant carriers: 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: 94
allele frequency: 5.694208868427429e-3
allele num: 16508
num of homozygotes: 3

Other
type: Population
allele count: 2
allele frequency: 2.207505518763797e-3
allele num: 906
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.729804532087874e-4
allele num: 11562
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.648784253184099e-5
allele num: 10364
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 126
allele frequency: 1.899650223133518e-3
allele num: 66328
num of homozygotes: 1

VQSLOD
type: SiteQuality
SIO_000300: 9.379999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.861875e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.507e0

MQ
type: SiteQuality
SIO_000300: 5.855e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.89e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.02e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.46e-1

FS
type: SiteQuality
SIO_000300: 5.5e-1

QD
type: SiteQuality
SIO_000300: 1.132e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.16e-1

GenotypeQuality
all individuals: 12692
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1869
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2217
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39345
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 805
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50793172085168e-5
allele num: 66316
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -1.413e0

FS
type: SiteQuality
SIO_000300: 7.362e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.49e0

DP
type: SiteQuality
SIO_000300: 1.847559e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.85e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.04e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.75e-1

QD
type: SiteQuality
SIO_000300: 1.252e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.52e-1

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

GenotypeQuality
all individuals: 27
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39318
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2757
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12689
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1868
bin: 9.75e1
variant carriers: 3

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.016409266409266e-5
allele num: 66304
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.861e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.39e0

QD
type: SiteQuality
SIO_000300: 1.156e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 4.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.41e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.492e0

MQRankSum
type: SiteQuality
SIO_000300: 1.3e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

DP
type: SiteQuality
SIO_000300: 1.847395e6

GenotypeQuality
all individuals: 2754
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 324
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1864
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 802
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 8.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
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: 1.508523155830442e-5
allele num: 66290
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.805e0

DP
type: SiteQuality
SIO_000300: 1.846991e6

BaseQRankSum
type: SiteQuality
SIO_000300: 9.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 9.54e-1

MQ
type: SiteQuality
SIO_000300: 5.676e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.25e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.71e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.388e0

QD
type: SiteQuality
SIO_000300: 1.465e1

GenotypeQuality
all individuals: 802
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 371
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12683
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509297271190534e-5
allele num: 66256
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.82e0

MQ
type: SiteQuality
SIO_000300: 4.239e1

FS
type: SiteQuality
SIO_000300: 2.806e0

DP
type: SiteQuality
SIO_000300: 1.84622e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -3.5e-1

QD
type: SiteQuality
SIO_000300: 1.404e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.81e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.804e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e0

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12673
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 801
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39235
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
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: 16504
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10332
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.53021654435082e-5
allele num: 66222
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

DP
type: SiteQuality
SIO_000300: 1.845054e6

QD
type: SiteQuality
SIO_000300: 1.449e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.93e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.046e0

FS
type: SiteQuality
SIO_000300: 6.13e-1

MQ
type: SiteQuality
SIO_000300: 5.822e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.39e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.75e0