Variant #0000608007 (NC_000002.11:g.47698108T>C, NM_000251.2:c.1666T>C (MSH2))
Chromosome |
2 |
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.47698108T>C |
DNA change (hg38) |
g.47470969T>C |
Published as |
MSH2(NM_000251.2):c.1666T>C (p.L556=, p.(Leu556=)), MSH2(NM_000251.3):c.1666T>C (p.L556=) |
ISCN |
- |
DB-ID |
MSH2_000564 See all 45 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) |
0.00434 View details |
Owner |
VKGL-NL_NKI |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_NKI |
Date created |
2019-12-04 14:54:23 +01:00 (CET) |
Date last edited |
2024-04-19 20:27:30 +02:00 (CEST) |

Variant on transcripts
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