Variant #0000618647 (NC_000022.10:g.50964255C>T, NM_001257988.1:c.1393G>A (TYMP))
Chromosome |
22 |
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.50964255C>T |
DNA change (hg38) |
g.50525826C>T |
Published as |
SCO2(NM_001169109.2):c.-14+420G>A, TYMP(NM_001113755.2):c.1393G>A (p.(Ala465Thr)) |
ISCN |
- |
DB-ID |
SCO2_000003 See all 3 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) |
0.04598 View details |
Owner |
VKGL-NL_Nijmegen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Nijmegen |
Date created |
2019-12-04 15:24:38 +01:00 (CET) |
Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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