Variant #0012368584 (NC_000020.10:g.62493061_62493069del, NM_199360.2:c.-3658_-3650del (TPD52L2))

Chromosome 20
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.62493061_62493069del
DB-ID -
dbSNP ID rs748685944
gnomAD frequency 11/67788
gnomAD homozygote count 0/33881
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.-3658_-3650del r.(=) p.(=)
TPD52L2 NM_001243892.1 ./. c.-3658_-3650del r.(=) p.(=)
TPD52L2 NM_001243894.1 ./. c.-3658_-3650del r.(=) p.(=)
TPD52L2 NM_001243895.1 ./. c.-3658_-3650del r.(=) p.(=)
TPD52L2 NM_003288.3 ./. c.-3658_-3650del r.(=) p.(=)
ABHD16B NM_080622.3 ./. c.168_176del r.(?) p.(Ala57_Val59del)
TPD52L2 NM_199359.2 ./. c.-3658_-3650del r.(=) p.(=)
TPD52L2 NM_199360.2 ./. c.-3658_-3650del r.(=) p.(=)
TPD52L2 NM_199361.2 ./. c.-3658_-3650del r.(=) p.(=)
TPD52L2 NM_199362.2 ./. c.-3658_-3650del r.(=) p.(=)
TPD52L2 NM_199363.2 ./. c.-3658_-3650del r.(=) p.(=)