Variant #0001035326 (NC_000005.9:g.79950749_79950750insGCCCCCAGCGCCCCCAGCGCCCCCAGC, NM_002439.4:c.203_204insGCCCCCAGCGCCCCCAGCGCCCCCAGC (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.79950749_79950750insGCCCCCAGCGCCCCCAGCGCCCCCAGC |
DNA change (hg38) |
- |
Published as |
DHFR(NM_000791.3):c.-420_-419insGGGGCGCTGGGGGCGCTGGGGGCGCTG (p.(=)), MSH3(NM_002439.5):c.203_204insGCCCCCAGCGCCCCCAGCGCCCCCAGC (p.P69_A70ins9) |
ISCN |
- |
DB-ID |
DHFR_000031 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) |
Retrieve |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2025-05-05 21:14:00 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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