Variant #0000588945 (NC_000005.9:g.140778130G>A, NC_000005.9(NM_018912.2):c.2421+65458G>A (PCDHGA1))

Chromosome 5
DNA change (genomic) (Relative to hg19 / GRCh37) g.140778130G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID PCDHGB4_000223
Frequency 2/12018
Freq. EA 0/8246
Freq. AA 2/3772
Average frequency (gnomAD v.2.1.1) -
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-05-03 16:26:58 +02:00 (CEST)
Date last edited 2013-05-04 07:47:01 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
PCDHGB4 NM_003736.2 ?/? c.2397+8282G>A r.(?) p.(Ala146Thr)
PCDHGA1 NM_018912.2 ?/? c.2421+65458G>A r.(?) p.(Ala146Thr)
PCDHGA2 NM_018915.2 ?/? c.2424+57168G>A r.(?) p.(Ala146Thr)
PCDHGA3 NM_018916.3 ?/? c.2424+52106G>A r.(?) p.(Ala146Thr)
PCDHGA4 NM_018917.2 ?/? c.2421+40942G>A r.(?) p.(Ala146Thr)
PCDHGA5 NM_018918.2 ?/? c.2421+31812G>A r.(?) p.(Ala146Thr)
PCDHGA6 NM_018919.2 ?/? c.2424+22056G>A r.(?) p.(Ala146Thr)
PCDHGA7 NM_018920.2 ?/? c.2424+13240G>A r.(?) p.(Ala146Thr)
PCDHGB1 NM_018922.2 ?/? c.2409+45894G>A r.(?) p.(Ala146Thr)
PCDHGB2 NM_018923.2 ?/? c.2421+36007G>A r.(?) p.(Ala146Thr)
PCDHGB3 NM_018924.2 ?/? c.2415+25754G>A r.(?) p.(Ala146Thr)
PCDHGB5 NM_018925.2 ?/? c.436G>A r.(?) p.(Ala146Thr)
PCDHGA8 NM_032088.1 ?/? c.2424+3326G>A r.(?) p.(Ala146Thr)