Variant #0012368555 (NC_000020.10:g.62492887A>C, NM_199360.2:c.-3832A>C (TPD52L2))

Chromosome 20
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.62492887A>C
DB-ID -
dbSNP ID rs745937528
gnomAD frequency 2/146196
gnomAD homozygote count 0/73096
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     
TPD52L2 NM_001243891.1 ./. c.-3832A>C r.(=) p.(=)
TPD52L2 NM_001243892.1 ./. c.-3832A>C r.(=) p.(=)
TPD52L2 NM_001243894.1 ./. c.-3832A>C r.(=) p.(=)
TPD52L2 NM_001243895.1 ./. c.-3832A>C r.(=) p.(=)
TPD52L2 NM_003288.3 ./. c.-3832A>C r.(=) p.(=)
ABHD16B NM_080622.3 ./. c.-7A>C r.(=) p.(=)
TPD52L2 NM_199359.2 ./. c.-3832A>C r.(=) p.(=)
TPD52L2 NM_199360.2 ./. c.-3832A>C r.(=) p.(=)
TPD52L2 NM_199361.2 ./. c.-3832A>C r.(=) p.(=)
TPD52L2 NM_199362.2 ./. c.-3832A>C r.(=) p.(=)
TPD52L2 NM_199363.2 ./. c.-3832A>C r.(=) p.(=)