Variant #0000311199 (NC_000001.10:g.33790580G>A, NM_198040.2:c.2463C>T (PHC2))

Chromosome 1
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.33790580G>A
DB-ID -
dbSNP ID rs370770593
gnomAD frequency 2/245652
gnomAD homozygote count 0/122824
Average frequency (gnomAD v.2.1.1) 1.0E-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.-3881C>T r.(=) p.(=)
PHC2 NM_004427.3 ./. c.858C>T r.(?) p.(Ile286=)
PHC2 NM_198040.2 ./. c.2463C>T r.(?) p.(Ile821=)