Variant #0000223293 (NC_000005.9:g.155771579T>C, NM_000337.5:c.84T>C (SGCD))
Chromosome |
5 |
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.155771579T>C |
DNA change (hg38) |
g.156344569T>C |
Published as |
- |
ISCN |
- |
DB-ID |
SGCD_000022 See all 14 reported entries |
Variant remarks |
- |
Reference |
from website {DBsub-Emory} |
ClinVar ID |
- |
dbSNP ID |
rs1801193 |
Origin |
Unknown |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.46782 View details |
Owner |
Madhuri Hegde |
Database submission license |
No license selected |
Created by |
Madhuri Hegde |
Date created |
2012-10-26 15:20:11 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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