Variant #0000420914 (NC_000002.11:g.47595033_47662777del, MSH2(NM_000251.2):c.-35298_1276+5697del)
Individual ID |
00195648 |
Chromosome |
2 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.47595033_47662777del |
DNA change (hg38) |
g.47367894_47435638del |
Published as |
Deletion of Exon 1-7 |
ISCN |
- |
DB-ID |
MSH2_000938 See all 4 reported entries |
Variant remarks |
- |
Reference |
PubMed: Nilbert 2002 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Michael Woods |
Database submission license |
No license selected |
Created by |
Michael Woods |

Variant on transcripts
Screenings
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