Variant #0000258842 (NC_000007.13:g.87079406T>A, NM_018849.2:c.711A>T (ABCB4))

Chromosome 7
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.87079406T>A
DNA change (hg38) g.87450090T>A
Published as ABCB4(NM_018849.3):c.711A>T (p.I237=)
ISCN -
DB-ID ABCB4_000023 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) 0.20705 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCB4 NM_000443.3 -/. - c.711A>T r.(?) p.(Ile237=)
ABCB4 NM_018849.2 -/. - c.711A>T r.(?) p.(Ile237=)


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