Variant #0000414225 (NC_000014.8:g.75516000A>G, NM_001040108.1:c.359T>C (MLH3))
| Chromosome |
14 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.75516000A>G |
| DNA change (hg38) |
g.75049297A>G |
| Published as |
- |
| ISCN |
- |
| DB-ID |
MLH3_000003 See all 4 reported entries |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Unknown |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00024 View details |
| Owner |
InSiGHT - John-Paul Plazzer |
| Database submission license |
No license selected |
| Created by |
Rina Kansal |
| Date created |
2014-07-07 21:45:00 +02:00 (CEST) |
| Date last edited |
2019-02-22 10:04:34 +01:00 (CET) |

Variant on transcripts
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