Variant #0000977872 (NC_000007.13:g.87173519C>T, NM_000927.4:c.2137G>A (ABCB1))

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.87173519C>T
DNA change (hg38) -
Published as ABCB1(NM_000927.5):c.2137G>A (p.V713I)
ISCN -
DB-ID ABCB1_000015
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCB1 NM_000927.4 ?/. - c.2137G>A r.(?) p.(Val713Ile)
ABCB1 NM_001348946.2 ?/. - c.2137G>A r.(?) p.(Val713Ile)
RUNDC3B NM_138290.2 ?/. - c.-84621C>T r.(?) p.(=)


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