Variant #0000622958 (NC_000012.11:g.6484669A>G, NC_000012.11(NM_001038.5):c.-55+2T>C (SCNN1A))
Chromosome |
12 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.6484669A>G |
DNA change (hg38) |
g.6375503A>G |
Published as |
SCNN1A(NM_001038.5):c.-55+2T>C, SCNN1A(NM_001038.6):c.-55+2T>C |
ISCN |
- |
DB-ID |
LTBR_000005 See all 2 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) |
Retrieve |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2019-12-06 12:43:26 +01:00 (CET) |
Date last edited |
2022-05-09 15:51:19 +02:00 (CEST) |

Variant on transcripts
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