Variant #0000526143 (NC_000005.9:g.79950724_79950732del, NM_002439.4:c.178_186del (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.79950724_79950732del |
DNA change (hg38) |
g.80654905_80654913del |
Published as |
DHFR(NM_000791.3):c.-409_-401del (p.(=)), DHFR(NM_000791.4):c.-409_-401delGGCCGCTGC, MSH3(NM_002439.4):c.178_186delGCCGCAGCG (p.A60_A62del), MSH3...) |
ISCN |
- |
DB-ID |
DHFR_000022 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_AMC |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_AMC |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2024-02-26 20:06:56 +01:00 (CET) |

Variant on transcripts
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