Variant #0000311198 (NC_000001.10:g.33790577G>A, NM_198040.2:c.2466C>T (PHC2))

Chromosome 1
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.33790577G>A
DB-ID -
dbSNP ID rs768182343
gnomAD frequency 8/245610
gnomAD homozygote count 0/122797
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
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     
A3GALT2 NM_001080438.1 ./. c.-3878C>T r.(=) p.(=)
PHC2 NM_004427.3 ./. c.861C>T r.(?) p.(Asp287=)
PHC2 NM_198040.2 ./. c.2466C>T r.(?) p.(Asp822=)