Variant #0000518169 (NC_000003.11:g.14207087T>C, XPC(NM_004628.4):c.622-2A>G)
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.14207087T>C |
DNA change (hg38) |
g.14165587T>C |
Published as |
XPC(NM_004628.4):c.622-2A>G |
ISCN |
- |
DB-ID |
XPC_000030 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) |
0 View details |
Owner |
VKGL-NL_Groningen |

Variant on transcripts
|
|