Variant #0000535552 (NC_000009.11:g.100437777T>C, NM_000380.3:c.766A>G (XPA))

Chromosome 9
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.100437777T>C
DNA change (hg38) g.97675495T>C
Published as XPA(NM_000380.4):c.766A>G (p.M256V)
ISCN -
DB-ID NCBP1_000002
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) 0.00211 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
XPA NM_000380.3 -/. - c.766A>G r.(?) p.(Met256Val)
NCBP1 NM_002486.4 -/. - c.*4296T>C r.(=) p.(=)
TSTD2 NM_139246.4 -/. - c.-42303A>G r.(?) p.(=)


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