Variant #0000506687 (NC_000001.10:g.243493867G>A, NM_006642.3:c.1094G>A (SDCCAG8))
Chromosome |
1 |
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.243493867G>A |
DNA change (hg38) |
g.243330565G>A |
Published as |
SDCCAG8(NM_001350251.1):c.191G>A (p.R64K), SDCCAG8(NM_006642.3):c.1094G>A (p.(Arg365Lys)), SDCCAG8(NM_006642.5):c.1094G>A (p.R365K) |
ISCN |
- |
DB-ID |
SDCCAG8_000035 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) |
0.0005 View details |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2022-05-09 15:24:52 +02:00 (CEST) |

Variant on transcripts
|