Variant #0000846970 (NC_000003.11:g.37067306G>A, NM_000249.3:c.1217G>A (MLH1))
Chromosome |
3 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
NA |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.37067306G>A |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
- |
DB-ID |
MLH1_000481 See all 64 reported entries |
Variant remarks |
Minigene splicing assay (pCAS2.MLH1.ex12): No splicing defect detected; Splicing predictions (MaxEntScan, SpliceSiteFinder-Like, SpliceAI): ΔMES= n.a. ΔSSFL= n.a. SpliceAI: no splicing defect predicted |
Reference |
PubMed: Tricarico et al 2017 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00088 View details |
Owner |
Alexandra Martins |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
InSiGHT - John-Paul Plazzer |
Date created |
2022-04-22 03:42:11 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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