Variant #0000526150 (NC_000005.9:g.79950732_79950733insGCCGCAGCGCCCGCAGCG, NM_002439.4:c.186_187insGCCGCAGCGCCCGCAGCG (MSH3))
Chromosome |
5 |
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.79950732_79950733insGCCGCAGCGCCCGCAGCG |
DNA change (hg38) |
g.80654913_80654914insGCCGCAGCGCCCGCAGCG |
Published as |
DHFR(NM_000791.3):c.-417_-416insGCGCTGCGGCCGCTGCGG (p.(=)), MSH3(NM_002439.4):c.186_187insGCCGCAGCGCCCGCAGCG (p.A62_P63insAAAPAA), MSH3(NM_002439....) |
ISCN |
- |
DB-ID |
MSH3_000009 See all 5 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) |
Retrieve |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2023-04-16 21:50:28 +02:00 (CEST) |

Variant on transcripts
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