Variant #0000612431 (NC_000010.10:g.21185962T>C, NC_000010.10(NM_006393.2):c.82-4A>G (NEBL))
Chromosome |
10 |
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.21185962T>C |
DNA change (hg38) |
g.20897033T>C |
Published as |
NEBL(NM_006393.2):c.82-4A>G |
ISCN |
- |
DB-ID |
C10orf113_000046 |
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) |
0.00024 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2019-12-04 15:24:38 +01:00 (CET) |
Date last edited |
2020-06-26 13:53:29 +02:00 (CEST) |

Variant on transcripts
|