Variant #0000850805 (NC_000005.9:g.140753671T>G, NC_000005.9(NM_018916.3):c.2424+27647T>G (PCDHGA3))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.140753671T>G
DNA change (hg38) -
Published as PCDHGA6(NM_018919.2):c.21T>G (p.H7Q)
ISCN -
DB-ID PCDHGA1_000083
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00016 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PCDHGC3 NM_002588.2 -?/. - c.-102013T>G r.(?) p.(=)
PCDHGA12 NM_003735.2 -?/. - c.-56656T>G r.(?) p.(=)
PCDHGB4 NM_003736.2 -?/. - c.-13781T>G r.(?) p.(=)
PCDHGA1 NM_018912.2 -?/. - c.2421+40999T>G r.(=) p.(=)
PCDHGA10 NM_018913.2 -?/. - c.-39072T>G r.(?) p.(=)
PCDHGA11 NM_018914.2 -?/. - c.-47124T>G r.(?) p.(=)
PCDHGA2 NM_018915.2 -?/. - c.2424+32709T>G r.(=) p.(=)
PCDHGA3 NM_018916.3 -?/. - c.2424+27647T>G r.(=) p.(=)
PCDHGA4 NM_018917.2 -?/. - c.2421+16483T>G r.(=) p.(=)
PCDHGA5 NM_018918.2 -?/. - c.2421+7353T>G r.(=) p.(=)
PCDHGA6 NM_018919.2 -?/. - c.21T>G r.(?) p.(His7Gln)
PCDHGA7 NM_018920.2 -?/. - c.-8796T>G r.(?) p.(=)
PCDHGA9 NM_018921.2 -?/. - c.-28849T>G r.(?) p.(=)
PCDHGB1 NM_018922.2 -?/. - c.2409+21435T>G r.(=) p.(=)
PCDHGB2 NM_018923.2 -?/. - c.2421+11548T>G r.(=) p.(=)
PCDHGB3 NM_018924.2 -?/. - c.2415+1295T>G r.(=) p.(=)
PCDHGB5 NM_018925.2 -?/. - c.-24024T>G r.(?) p.(=)
PCDHGB6 NM_018926.2 -?/. - c.-34099T>G r.(?) p.(=)
PCDHGB7 NM_018927.3 -?/. - c.-43756T>G r.(?) p.(=)
PCDHGC4 NM_018928.2 -?/. - c.-111070T>G r.(?) p.(=)
PCDHGC5 NM_018929.2 -?/. - c.-115137T>G r.(?) p.(=)
PCDHGA8 NM_032088.1 -?/. - c.-18710T>G r.(?) p.(=)


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