Variant #0000515900 (NC_000002.11:g.44066227C>T, NM_022437.2:c.35C>T (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.44066227C>T
DNA change (hg38) g.43839088C>T
Published as ABCG8(NM_022437.3):c.35C>T (p.P12L)
ISCN -
DB-ID ABCG5_000122
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) 3.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCG5 NM_022436.2 ?/. - c.-409G>A r.(?) p.(=)
ABCG8 NM_022437.2 ?/. - c.35C>T r.(?) p.(Pro12Leu)


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