Variant #0000924765 (NC_000007.13:g.87101932C>A, NC_000007.13(NM_018849.2):c.135+5G>T (ABCB4))

Chromosome 7
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.87101932C>A
DNA change (hg38) -
Published as ABCB4(NM_000443.4):c.135+5G>T
ISCN -
DB-ID ABCB4_000086
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 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCB4 NM_000443.3 ?/. - c.135+5G>T r.spl? p.?
ABCB4 NM_018849.2 ?/. - c.135+5G>T r.spl? p.?


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