Variant #0000535553 (NC_000009.11:g.100437812T>C, NM_000380.3:c.731A>G (XPA))

Chromosome 9
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.100437812T>C
DNA change (hg38) g.97675530T>C
Published as XPA(NM_000380.3):c.731A>G (p.H244R), XPA(NM_001354975.2):c.605A>G (p.H202R)
ISCN -
DB-ID XPA_000009 See all 4 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00013 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
XPA NM_000380.3 ?/. - c.731A>G r.(?) p.(His244Arg)
NCBP1 NM_002486.4 ?/. - c.*4331T>C r.(=) p.(=)
TSTD2 NM_139246.4 ?/. - c.-42338A>G r.(?) p.(=)


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