Variant #0000313637 (NC_000009.11:g.35059790T>C, VCP(NM_007126.3):c.1704A>G)
Chromosome |
9 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.35059790T>C |
DNA change (hg38) |
g.35059793T>C |
Published as |
VCP(NM_001354928.1):c.1569A>G (p.Q523=), VCP(NM_007126.3):c.1704A>G (p.Q568=), VCP(NM_007126.5):c.1704A>G (p.Q568=) |
ISCN |
- |
DB-ID |
VCP_000031 See all 4 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) |
0.00272 View details |
Owner |
VKGL-NL_VUmc |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_VUmc |

Variant on transcripts
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