Variant #0000518156 (NC_000003.11:g.14199542A>G, XPC(NM_004628.4):c.1841T>C)
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.14199542A>G |
DNA change (hg38) |
g.14158042A>G |
Published as |
XPC(NM_004628.4):c.1841T>C (p.F614S) |
ISCN |
- |
DB-ID |
XPC_000019 |
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) |
0.00152 View details |
Owner |
VKGL-NL_Rotterdam |

Variant on transcripts
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