Variant #0002547837 (NC_000003.11:g.52003490T>C, NM_001174100.1:c.-2361A>G (PCBP4))

Chromosome 3
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.52003490T>C
DB-ID -
dbSNP ID rs745745778
gnomAD frequency 14/245132
gnomAD homozygote count 0/122552
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     
ABHD14B NM_001146314.1 ./. c.585A>G r.(?) p.(Pro195=)
PCBP4 NM_001174100.1 ./. c.-2361A>G r.(=) p.(=)
ABHD14B NM_001254753.1 ./. c.471A>G r.(?) p.(Pro157=)
PCBP4 NM_020418.3 ./. c.-2296A>G r.(=) p.(=)
ABHD14B NM_032750.2 ./. c.585A>G r.(?) p.(Pro195=)
PCBP4 NM_033008.2 ./. c.-2213A>G r.(=) p.(=)
ABHD14A XM_005265018.1 ./. c.-4378T>C r.(=) p.(=)