Variant #0000518170 (NC_000003.11:g.14209872_14209875del, XPC(NM_004628.4):c.420_423del)
Chromosome |
3 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.14209872_14209875del |
DNA change (hg38) |
g.14168372_14168375del |
Published as |
XPC(NM_004628.4):c.420_423del (p.(Glu141LeufsTer6)), XPC(NM_004628.4):c.420_423delTGAG (p.E141Lfs*6) |
ISCN |
- |
DB-ID |
XPC_000012 See all 2 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) |
Variant not found in online data sets |
Owner |
VKGL-NL_Leiden |

Variant on transcripts
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