Variant #0001052132 (NC_000005.9:g.140890603G>A, NM_005219.4:c.*5815C>T (DIAPH1))

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.140890603G>A
DNA change (hg38) -
Published as PCDHGC4(NM_018928.3):c.2680G>A (p.(Val894Met))
ISCN -
DB-ID DIAPH1_000131
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) 4.0E-5 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 2025-11-01 13:22:20 +01:00 (CET)
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.2668G>A r.(?) p.(Val890Met)
PCDHGA12 NM_003735.2 ?/. - c.2662G>A r.(?) p.(Val888Met)
PCDHGB4 NM_003736.2 ?/. - c.2635G>A r.(?) p.(Val879Met)
DIAPH1 NM_005219.4 ?/. - c.*5815C>T r.(=) p.(=)
PCDHGA1 NM_018912.2 ?/. - c.2659G>A r.(?) p.(Val887Met)
PCDHGA10 NM_018913.2 ?/. - c.2674G>A r.(?) p.(Val892Met)
PCDHGA11 NM_018914.2 ?/. - c.2671G>A r.(?) p.(Val891Met)
PCDHGA2 NM_018915.2 ?/. - c.2662G>A r.(?) p.(Val888Met)
PCDHGA3 NM_018916.3 ?/. - c.2662G>A r.(?) p.(Val888Met)
PCDHGA4 NM_018917.2 ?/. - c.2659G>A r.(?) p.(Val887Met)
PCDHGA5 NM_018918.2 ?/. - c.2659G>A r.(?) p.(Val887Met)
PCDHGA6 NM_018919.2 ?/. - c.2662G>A r.(?) p.(Val888Met)
PCDHGA7 NM_018920.2 ?/. - c.2662G>A r.(?) p.(Val888Met)
PCDHGA9 NM_018921.2 ?/. - c.2662G>A r.(?) p.(Val888Met)
PCDHGB1 NM_018922.2 ?/. - c.2647G>A r.(?) p.(Val883Met)
PCDHGB2 NM_018923.2 ?/. - c.2659G>A r.(?) p.(Val887Met)
PCDHGB3 NM_018924.2 ?/. - c.2653G>A r.(?) p.(Val885Met)
PCDHGB5 NM_018925.2 ?/. - c.2635G>A r.(?) p.(Val879Met)
PCDHGB6 NM_018926.2 ?/. - c.2656G>A r.(?) p.(Val886Met)
PCDHGB7 NM_018927.3 ?/. - c.2653G>A r.(?) p.(Val885Met)
PCDHGC4 NM_018928.2 ?/. - c.2680G>A r.(?) p.(Val894Met)
PCDHGC5 NM_018929.2 ?/. - c.2698G>A r.(?) p.(Val900Met)
PCDHGA8 NM_032088.1 ?/. - c.2662G>A r.(?) p.(Val888Met)


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