Variant #0000330571 (NC_000005.9:g.140223058T>C, NC_000005.9(NM_018900.2):c.2394+54789T>C (PCDHA1))

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.140223058T>C
DNA change (hg38) -
Published as PCDHA8(NM_018911.2):c.2152T>C (p.(Tyr718His))
ISCN -
DB-ID PCDHA1_000011
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) 0.00073 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 2018-01-15 20:58:59 +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     
PCDHAC1 NM_018898.3 ?/. - c.-83420T>C r.(?) p.(=)
PCDHAC2 NM_018899.5 ?/. - c.-123294T>C r.(?) p.(=)
PCDHA1 NM_018900.2 ?/. - c.2394+54789T>C r.(=) p.(=)
PCDHA10 NM_018901.2 ?/. - c.-12576T>C r.(?) p.(=)
PCDHA11 NM_018902.3 ?/. - c.-25631T>C r.(?) p.(=)
PCDHA12 NM_018903.2 ?/. - c.-32000T>C r.(?) p.(=)
PCDHA13 NM_018904.2 ?/. - c.-38796T>C r.(?) p.(=)
PCDHA2 NM_018905.2 ?/. - c.2388+46121T>C r.(=) p.(=)
PCDHA3 NM_018906.2 ?/. - c.2394+39882T>C r.(=) p.(=)
PCDHA4 NM_018907.2 ?/. - c.2385+33901T>C r.(=) p.(=)
PCDHA5 NM_018908.2 ?/. - c.2352+19346T>C r.(=) p.(=)
PCDHA6 NM_018909.2 ?/. - c.2394+12988T>C r.(=) p.(=)
PCDHA7 NM_018910.2 ?/. - c.2355+6735T>C r.(=) p.(=)
PCDHA8 NM_018911.2 ?/. - c.2152T>C r.(?) p.(Tyr718His)
PCDHA9 NM_031857.1 ?/. - c.-5023T>C r.(?) p.(=)


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