Variant #0000680046 (NC_000014.8:g.75516351T>C, NM_001040108.1:c.8A>G (MLH3))
| Chromosome |
14 |
| 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.75516351T>C |
| DNA change (hg38) |
- |
| Published as |
MLH3(NM_001040108.1):c.8A>G (p.(Lys3Arg)), MLH3(NM_001040108.2):c.8A>G (p.K3R) |
| ISCN |
- |
| DB-ID |
ACYP1_000002 See all 4 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) |
0.00221 View details |
| Owner |
VKGL-NL_AMC |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_AMC |
| Date created |
2020-08-06 14:59:34 +02:00 (CEST) |
| Date last edited |
2023-11-27 17:27:23 +01:00 (CET) |

Variant on transcripts
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