Variant #0000321177 (NC_000001.10:g.186034508T>C, NM_031935.2:c.7652T>C (HMCN1))
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.186034508T>C |
DNA change (hg38) |
g.186065376T>C |
Published as |
HMCN1(NM_031935.2):c.7652T>C (p.(Leu2551Ser)), HMCN1(NM_031935.3):c.7652T>C (p.L2551S) |
ISCN |
- |
DB-ID |
HMCN1_000032 See all 2 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) |
0.00112 View details |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2024-10-29 20:49:11 +01:00 (CET) |

Variant on transcripts
|