Variant #0000994713 (NC_000005.9:g.140774072C>A, NC_000005.9(NM_018916.3):c.2424+48048C>A (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.140774072C>A
DNA change (hg38) -
Published as PCDHGA8(NM_032088.1):c.1692C>A (p.(Tyr564*))
ISCN -
DB-ID PCDHGA1_000091
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 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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.-81612C>A r.(?) p.(=)
PCDHGA12 NM_003735.2 ?/. - c.-36255C>A r.(?) p.(=)
PCDHGB4 NM_003736.2 ?/. - c.2397+4224C>A r.(=) p.(=)
PCDHGA1 NM_018912.2 ?/. - c.2421+61400C>A r.(=) p.(=)
PCDHGA10 NM_018913.2 ?/. - c.-18671C>A r.(?) p.(=)
PCDHGA11 NM_018914.2 ?/. - c.-26723C>A r.(?) p.(=)
PCDHGA2 NM_018915.2 ?/. - c.2424+53110C>A r.(=) p.(=)
PCDHGA3 NM_018916.3 ?/. - c.2424+48048C>A r.(=) p.(=)
PCDHGA4 NM_018917.2 ?/. - c.2421+36884C>A r.(=) p.(=)
PCDHGA5 NM_018918.2 ?/. - c.2421+27754C>A r.(=) p.(=)
PCDHGA6 NM_018919.2 ?/. - c.2424+17998C>A r.(=) p.(=)
PCDHGA7 NM_018920.2 ?/. - c.2424+9182C>A r.(=) p.(=)
PCDHGA9 NM_018921.2 ?/. - c.-8448C>A r.(?) p.(=)
PCDHGB1 NM_018922.2 ?/. - c.2409+41836C>A r.(=) p.(=)
PCDHGB2 NM_018923.2 ?/. - c.2421+31949C>A r.(=) p.(=)
PCDHGB3 NM_018924.2 ?/. - c.2415+21696C>A r.(=) p.(=)
PCDHGB5 NM_018925.2 ?/. - c.-3623C>A r.(?) p.(=)
PCDHGB6 NM_018926.2 ?/. - c.-13698C>A r.(?) p.(=)
PCDHGB7 NM_018927.3 ?/. - c.-23355C>A r.(?) p.(=)
PCDHGC4 NM_018928.2 ?/. - c.-90669C>A r.(?) p.(=)
PCDHGC5 NM_018929.2 ?/. - c.-94736C>A r.(?) p.(=)
PCDHGA8 NM_032088.1 ?/. - c.1692C>A r.(?) p.(Tyr564*)


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