Variant #0000331970 (NC_000007.13:g.150912148C>A, ABCF2(NM_005692.3):c.1551G>T)

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.150912148C>A
DNA change (hg38) g.151215062C>A
Published as ABCF2(NM_005692.3):c.1551G>T (p.(Leu517Phe))
ISCN -
DB-ID ABCF2_000001
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCF2 NM_005692.3 ?/. - c.1551G>T r.(?) p.(Leu517Phe)