Variant #0000312991 (NC_000009.11:g.35060302T>C, VCP(NM_007126.3):c.1695+8A>G)
Chromosome |
9 |
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.35060302T>C |
DNA change (hg38) |
g.35060305T>C |
Published as |
VCP(NM_001354928.2):c.1560+8A>G, VCP(NM_007126.3):c.1695+8A>G, VCP(NM_007126.5):c.1695+8A>G |
ISCN |
- |
DB-ID |
VCP_000033 See all 6 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) |
0.59295 View details |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |

Variant on transcripts
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