Variant #0012368587 (NC_000020.10:g.62493063C>T, NM_199360.2:c.-3656C>T (TPD52L2))

Chromosome 20
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.62493063C>T
DB-ID -
dbSNP ID rs767457694
gnomAD frequency 4/65698
gnomAD homozygote count 1/32833
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.-3656C>T r.(=) p.(=)
TPD52L2 NM_001243892.1 ./. c.-3656C>T r.(=) p.(=)
TPD52L2 NM_001243894.1 ./. c.-3656C>T r.(=) p.(=)
TPD52L2 NM_001243895.1 ./. c.-3656C>T r.(=) p.(=)
TPD52L2 NM_003288.3 ./. c.-3656C>T r.(=) p.(=)
ABHD16B NM_080622.3 ./. c.170C>T r.(?) p.(Ala57Val)
TPD52L2 NM_199359.2 ./. c.-3656C>T r.(=) p.(=)
TPD52L2 NM_199360.2 ./. c.-3656C>T r.(=) p.(=)
TPD52L2 NM_199361.2 ./. c.-3656C>T r.(=) p.(=)
TPD52L2 NM_199362.2 ./. c.-3656C>T r.(=) p.(=)
TPD52L2 NM_199363.2 ./. c.-3656C>T r.(=) p.(=)