Variant #0012368851 (NC_000020.10:g.62494008T>C, NM_199360.2:c.-2711T>C (TPD52L2))

Chromosome 20
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.62494008T>C
DB-ID -
dbSNP ID -
gnomAD frequency 2/132354
gnomAD homozygote count 0/66174
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     
TPD52L2 NM_001243891.1 ./. c.-2711T>C r.(=) p.(=)
TPD52L2 NM_001243892.1 ./. c.-2711T>C r.(=) p.(=)
TPD52L2 NM_001243894.1 ./. c.-2711T>C r.(=) p.(=)
TPD52L2 NM_001243895.1 ./. c.-2711T>C r.(=) p.(=)
TPD52L2 NM_003288.3 ./. c.-2711T>C r.(=) p.(=)
ABHD16B NM_080622.3 ./. c.1115delTinsC r.(?) p.(Leu372Pro)
TPD52L2 NM_199359.2 ./. c.-2711T>C r.(=) p.(=)
TPD52L2 NM_199360.2 ./. c.-2711T>C r.(=) p.(=)
TPD52L2 NM_199361.2 ./. c.-2711T>C r.(=) p.(=)
TPD52L2 NM_199362.2 ./. c.-2711T>C r.(=) p.(=)
TPD52L2 NM_199363.2 ./. c.-2711T>C r.(=) p.(=)