Variant #0000974990 (NC_000002.11:g.220077210_220077211insACCTGTT, NM_005689.2:c.1866_1867insAACAGGT (ABCB6))

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.220077210_220077211insACCTGTT
DNA change (hg38) -
Published as ABCB6(NM_005689.4):c.1866_1867insAACAGGT (p.(Gly623Asnfs*57))
ISCN -
DB-ID ABCB6_000062
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) 4.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:20:39 +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     
ABCB6 NM_005689.2 ?/. - c.1866_1867insAACAGGT r.(?) p.(Gly623Asnfs*57)
ZFAND2B NM_138802.2 ?/. - c.*3182_*3183insACCTGTT r.(=) p.(=)


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