Variant #0002547822 (NC_000003.11:g.52003441T>G, NM_001174100.1:c.-2312A>C (PCBP4))

Chromosome 3
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.52003441T>G
DB-ID -
dbSNP ID rs752198689
gnomAD frequency 2/242674
gnomAD homozygote count 0/121335
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABHD14B NM_001146314.1 ./. c.*1A>C r.(=) p.(=)
PCBP4 NM_001174100.1 ./. c.-2312A>C r.(=) p.(=)
ABHD14B NM_001254753.1 ./. c.*1A>C r.(=) p.(=)
PCBP4 NM_020418.3 ./. c.-2247A>C r.(=) p.(=)
ABHD14B NM_032750.2 ./. c.*1A>C r.(=) p.(=)
PCBP4 NM_033008.2 ./. c.-2164A>C r.(=) p.(=)
ABHD14A XM_005265018.1 ./. c.-4427T>G r.(=) p.(=)