Variant #0000520731 (NC_000003.11:g.87299075A>C, NM_014043.3:c.372A>C (CHMP2B))
Chromosome |
3 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.87299075A>C |
DNA change (hg38) |
g.87249925A>C |
Published as |
CHMP2B(NM_014043.3):c.372A>C (p.T124=), CHMP2B(NM_014043.4):c.372A>C (p.T124=) |
ISCN |
- |
DB-ID |
CHMP2B_000012 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) |
0.09375 View details |
Owner |
VKGL-NL_VUmc |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_VUmc |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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