Variant #0000858358 (NC_000002.11:g.220079136A>G, NM_005689.2:c.1361T>C (ABCB6))

Chromosome 2
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.220079136A>G
DNA change (hg38) -
Published as ABCB6(NM_005689.2):c.1361T>C (p.(Val454Ala)), ABCB6(NM_005689.4):c.1361T>C (p.V454A)
ISCN -
DB-ID ABCB6_000012 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) 0.00613 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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2024-08-28 13:07:21 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCB6 NM_005689.2 -/. - c.1361T>C r.(?) p.(Val454Ala)
ATG9A NM_024085.3 -/. - c.*6033T>C r.(=) p.(=)
ZFAND2B NM_138802.2 -/. - c.*5108A>G r.(=) p.(=)


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