Variant #0000609535 (NC_000005.9:g.140732226T>C, NC_000005.9(NM_018916.3):c.2424+6202T>C (PCDHGA3))

Chromosome 5
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.140732226T>C
DNA change (hg38) -
Published as PCDHGB1(NM_018922.2):c.2399T>C (p.L800S)
ISCN -
DB-ID PCDHGA1_000073
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) 0.00014 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PCDHGC3 NM_002588.2 ?/. - c.-123458T>C r.(?) p.(=)
PCDHGA12 NM_003735.2 ?/. - c.-78101T>C r.(?) p.(=)
PCDHGB4 NM_003736.2 ?/. - c.-35226T>C r.(?) p.(=)
PCDHGA1 NM_018912.2 ?/. - c.2421+19554T>C r.(=) p.(=)
PCDHGA10 NM_018913.2 ?/. - c.-60517T>C r.(?) p.(=)
PCDHGA11 NM_018914.2 ?/. - c.-68569T>C r.(?) p.(=)
PCDHGA2 NM_018915.2 ?/. - c.2424+11264T>C r.(=) p.(=)
PCDHGA3 NM_018916.3 ?/. - c.2424+6202T>C r.(=) p.(=)
PCDHGA4 NM_018917.2 ?/. - c.-2542T>C r.(?) p.(=)
PCDHGA5 NM_018918.2 ?/. - c.-11672T>C r.(?) p.(=)
PCDHGA6 NM_018919.2 ?/. - c.-21425T>C r.(?) p.(=)
PCDHGA7 NM_018920.2 ?/. - c.-30241T>C r.(?) p.(=)
PCDHGA9 NM_018921.2 ?/. - c.-50294T>C r.(?) p.(=)
PCDHGB1 NM_018922.2 ?/. - c.2399T>C r.(?) p.(Leu800Ser)
PCDHGB2 NM_018923.2 ?/. - c.-7477T>C r.(?) p.(=)
PCDHGB3 NM_018924.2 ?/. - c.-17736T>C r.(?) p.(=)
PCDHGB5 NM_018925.2 ?/. - c.-45469T>C r.(?) p.(=)
PCDHGB6 NM_018926.2 ?/. - c.-55544T>C r.(?) p.(=)
PCDHGB7 NM_018927.3 ?/. - c.-65201T>C r.(?) p.(=)
PCDHGC4 NM_018928.2 ?/. - c.-132515T>C r.(?) p.(=)
PCDHGC5 NM_018929.2 ?/. - c.-136582T>C r.(?) p.(=)
PCDHGA8 NM_032088.1 ?/. - c.-40155T>C r.(?) p.(=)


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