Variant #0000514693 (NC_000002.11:g.220081167C>A, ABCB6(NM_005689.2):c.889G>T)

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.220081167C>A
DNA change (hg38) g.219216445C>A
Published as ABCB6(NM_005689.2):c.889G>T (p.A297S)
ISCN -
DB-ID ABCB6_000027
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) Variant not found in online data sets
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCB6 NM_005689.2 ?/. - c.889G>T r.(?) p.(Ala297Ser)
ATG9A NM_024085.3 ?/. - c.*4002G>T r.(=) p.(=)