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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