Variant #0008572849 (NC_000013.10:g.95696668C>T, NM_005845.3:c.3481delGinsA (ABCC4))

Chromosome 13
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.95696668C>T
DB-ID -
dbSNP ID rs747462604
gnomAD frequency 1/243846
gnomAD homozygote count 0/121921
Average frequency (gnomAD v.2.1.1) Retrieve
Database submission license No license selected
Created by LOVD
Date created 2017-02-27 00:00:00 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCC4 NM_005845.3 ./. c.3481delGinsA r.(?) p.(Asp1161Asn)