Variant #0002691378 (NC_000003.11:g.111693338G>A, NM_001134437.1:c.3642G>A (PHLDB2))

Chromosome 3
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.111693338G>A
DB-ID -
dbSNP ID rs142225277
gnomAD frequency 1/245880
gnomAD homozygote count 0/122928
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     
PHLDB2 NM_001134437.1 ./. c.3642G>A r.(?) p.(Ser1214=)
PHLDB2 NM_001134438.1 ./. c.3690G>A r.(?) p.(Ser1230=)
PHLDB2 NM_001134439.1 ./. c.3690G>A r.(?) p.(Ser1230=)
ABHD10 NM_001272069.1 ./. c.-4571G>A r.(=) p.(=)
ABHD10 NM_018394.3 ./. c.-4571G>A r.(=) p.(=)
PHLDB2 NM_145753.2 ./. c.3561G>A r.(?) p.(Ser1187=)