Variant #0000535551 (NC_000009.11:g.100437769dup, NM_000380.3:c.774dup (XPA))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.100437769dup
DNA change (hg38) g.97675487dup
Published as XPA(NM_000380.3):c.774dupT (p.K259*)
ISCN -
DB-ID NCBP1_000001
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) Retrieve
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 2020-06-25 16:46:00 +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.774dup r.(?) p.(Lys259Ter)
NCBP1 NM_002486.4 +?/. - c.*4288dup r.(?) p.(=)
TSTD2 NM_139246.4 +?/. - c.-42295dup r.(?) p.(=)


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