Variant #0000518165 (NC_000003.11:g.14206353A>C, XPC(NM_004628.4):c.860T>G)
Chromosome |
3 |
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.14206353A>C |
DNA change (hg38) |
g.14164853A>C |
Published as |
XPC(NM_001145769.1):c.749T>G (p.(Phe250Cys)), XPC(NM_004628.4):c.860T>G (p.F287C) |
ISCN |
- |
DB-ID |
XPC_000028 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) |
0.00137 View details |
Owner |
VKGL-NL_Rotterdam |

Variant on transcripts
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