Variant #0000610365 (NC_000006.11:g.43413555C>T, NM_033450.2:c.3165C>T (ABCC10))
Chromosome |
6 |
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.43413555C>T |
DNA change (hg38) |
g.43445817C>T |
Published as |
ABCC10(NM_033450.2):c.3165C>T (p.R1055=) |
ISCN |
- |
DB-ID |
ABCC10_000005 |
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) |
8.0E-5 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2019-12-04 15:24:38 +01:00 (CET) |
Date last edited |
2020-06-19 13:32:10 +02:00 (CEST) |

Variant on transcripts
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