Variant #0000976605 (NC_000005.9:g.140890595T>G, NM_005219.4:c.*5823A>C (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.140890595T>G
DNA change (hg38) -
Published as PCDHGC4(NM_018928.3):c.2672T>G (p.(Leu891Arg))
ISCN -
DB-ID DIAPH1_000121
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 2024-04-19 20:27:30 +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.2660T>G r.(?) p.(Leu887Arg)
PCDHGA12 NM_003735.2 ?/. - c.2654T>G r.(?) p.(Leu885Arg)
PCDHGB4 NM_003736.2 ?/. - c.2627T>G r.(?) p.(Leu876Arg)
DIAPH1 NM_005219.4 ?/. - c.*5823A>C r.(=) p.(=)
PCDHGA1 NM_018912.2 ?/. - c.2651T>G r.(?) p.(Leu884Arg)
PCDHGA10 NM_018913.2 ?/. - c.2666T>G r.(?) p.(Leu889Arg)
PCDHGA11 NM_018914.2 ?/. - c.2663T>G r.(?) p.(Leu888Arg)
PCDHGA2 NM_018915.2 ?/. - c.2654T>G r.(?) p.(Leu885Arg)
PCDHGA3 NM_018916.3 ?/. - c.2654T>G r.(?) p.(Leu885Arg)
PCDHGA4 NM_018917.2 ?/. - c.2651T>G r.(?) p.(Leu884Arg)
PCDHGA5 NM_018918.2 ?/. - c.2651T>G r.(?) p.(Leu884Arg)
PCDHGA6 NM_018919.2 ?/. - c.2654T>G r.(?) p.(Leu885Arg)
PCDHGA7 NM_018920.2 ?/. - c.2654T>G r.(?) p.(Leu885Arg)
PCDHGA9 NM_018921.2 ?/. - c.2654T>G r.(?) p.(Leu885Arg)
PCDHGB1 NM_018922.2 ?/. - c.2639T>G r.(?) p.(Leu880Arg)
PCDHGB2 NM_018923.2 ?/. - c.2651T>G r.(?) p.(Leu884Arg)
PCDHGB3 NM_018924.2 ?/. - c.2645T>G r.(?) p.(Leu882Arg)
PCDHGB5 NM_018925.2 ?/. - c.2627T>G r.(?) p.(Leu876Arg)
PCDHGB6 NM_018926.2 ?/. - c.2648T>G r.(?) p.(Leu883Arg)
PCDHGB7 NM_018927.3 ?/. - c.2645T>G r.(?) p.(Leu882Arg)
PCDHGC4 NM_018928.2 ?/. - c.2672T>G r.(?) p.(Leu891Arg)
PCDHGC5 NM_018929.2 ?/. - c.2690T>G r.(?) p.(Leu897Arg)
PCDHGA8 NM_032088.1 ?/. - c.2654T>G r.(?) p.(Leu885Arg)


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