Variant #0000346194 (NC_000011.9:g.68673631G>C, NM_002180.2:c.181G>C (IGHMBP2))
Chromosome |
11 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.68673631G>C |
DNA change (hg38) |
g.68906163G>C |
Published as |
IGHMBP2(NM_002180.2):c.181G>C (p.(Gly61Arg)), IGHMBP2(NM_002180.3):c.181G>C (p.G61R) |
ISCN |
- |
DB-ID |
IGHMBP2_000103 See all 3 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) |
1.0E-5 View details |
Owner |
VKGL-NL_Nijmegen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Nijmegen |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2023-07-07 10:10:56 +02:00 (CEST) |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|