Variant #0000607953 (NC_000002.11:g.44066194T>C, NM_022437.2:c.2T>C (ABCG8))
Chromosome |
2 |
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.44066194T>C |
DNA change (hg38) |
g.43839055T>C |
Published as |
ABCG8(NM_022437.3):c.2T>C (p.M1?) |
ISCN |
- |
DB-ID |
ABCG5_000152 |
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) |
0.00019 View details |
Owner |
VKGL-NL_AMC |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_AMC |
Date created |
2019-12-04 14:54:23 +01:00 (CET) |
Date last edited |
2020-06-08 14:39:43 +02:00 (CEST) |

Variant on transcripts
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