Variant #0000703842 (NC_000010.10:g.43600496C>T, NM_020975.4:c.722C>T (RET))
Chromosome |
10 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.43600496C>T |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
- |
DB-ID |
RET_000293 |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs1178140696 |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
MobiDetails |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
MobiDetails |
Date created |
2020-11-09 14:53:02 +01:00 (CET) |
Date last edited |
2022-09-26 12:22:42 +02:00 (CEST) |

Variant on transcripts
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