Variant #0000223259 (NC_000017.10:g.48252804C>T, NM_000023.2:c.*6C>T (SGCA))
Chromosome |
17 |
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.48252804C>T |
DNA change (hg38) |
g.50175443C>T |
Published as |
*6T>C |
ISCN |
- |
DB-ID |
SGCA_000047 See all 6 reported entries |
Variant remarks |
Variant Error [EREF/EREF]: This genomic variant does not match the reference sequence; the transcript variant does not match the reference sequence either. Please fix this entry and then remove this message. |
Reference |
from website {DBsub-Emory} |
ClinVar ID |
- |
dbSNP ID |
rs2696288 |
Origin |
Germline |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Madhuri Hegde |
Database submission license |
No license selected |
Created by |
Madhuri Hegde |
Date created |
2012-10-26 15:17:26 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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