Variant #0000679641 (NC_000012.11:g.7177172C>G, NM_001734.3:c.1284C>G (C1S))
Chromosome |
12 |
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.7177172C>G |
DNA change (hg38) |
- |
Published as |
C1S(NM_001734.3):c.1284C>G (p.P428=), C1S(NM_001734.5):c.1284C>G (p.P428=), C1S(NM_201442.3):c.1284C>G (p.P428=) |
ISCN |
- |
DB-ID |
C1S_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) |
0.00089 View details |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2020-08-06 14:59:34 +02:00 (CEST) |
Date last edited |
2023-04-16 21:50:28 +02:00 (CEST) |

Variant on transcripts
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