Variant #0000565595 (NC_000019.9:g.1053459C>T, ABCA7(NM_019112.3):c.3352C>T)

Chromosome 19
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.1053459C>T
DNA change (hg38) g.1053460C>T
Published as ABCA7(NM_019112.3):c.3352C>T (p.(Arg1118Ter))
ISCN -
DB-ID ABCA7_000030
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) 1.0E-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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCA7 NM_019112.3 ?/. - c.3352C>T r.(?) p.(Arg1118Ter)