Variant #0000290876 (NC_000004.11:g.113568478C>A, C4orf21(NM_018392.4):c.-10538G>T)
Chromosome |
4 |
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.113568478C>A |
DNA change (hg38) |
g.112647322C>A |
Published as |
LARP7(NM_001267039.1):c.791C>A (p.T264K) |
ISCN |
- |
DB-ID |
LARP7_000005 |
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_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |

Variant on transcripts
|
|