Variant #0000546111 (NC_000011.9:g.94212884T>C, NM_005591.3:c.358A>G (MRE11A))
Chromosome |
11 |
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.94212884T>C |
DNA change (hg38) |
g.94479718T>C |
Published as |
MRE11(NM_001330347.1):c.358A>G (p.I120V), MRE11A(NM_005590.3):c.358A>G (p.(Ile120Val)) |
ISCN |
- |
DB-ID |
MRE11A_000038 See all 4 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) |
5.0E-5 View details |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2019-12-06 12:43:26 +01:00 (CET) |

Variant on transcripts
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