Variant #0000524492 (NC_000005.9:g.140255760G>A, NC_000005.9(NM_018900.2):c.2394+87491G>A (PCDHA1))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.140255760G>A
DNA change (hg38) -
Published as PCDHA12(NM_018903.3):c.703G>A (p.(Val235Met)), PCDHA12(NM_018903.4):c.703G>A (p.V235M)
ISCN -
DB-ID PCDHA1_000052 See all 2 reported entries
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2019-12-04 15:24:38 +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.-50718G>A r.(?) p.(=)
PCDHAC2 NM_018899.5 -?/. - c.-90592G>A r.(?) p.(=)
PCDHA1 NM_018900.2 -?/. - c.2394+87491G>A r.(=) p.(=)
PCDHA10 NM_018901.2 -?/. - c.2388+17739G>A r.(=) p.(=)
PCDHA11 NM_018902.3 -?/. - c.2391+4681G>A r.(=) p.(=)
PCDHA12 NM_018903.2 -?/. - c.703G>A r.(?) p.(Val235Met)
PCDHA13 NM_018904.2 -?/. - c.-6094G>A r.(?) p.(=)
PCDHA2 NM_018905.2 -?/. - c.2388+78823G>A r.(=) p.(=)
PCDHA3 NM_018906.2 -?/. - c.2394+72584G>A r.(=) p.(=)
PCDHA4 NM_018907.2 -?/. - c.2385+66603G>A r.(=) p.(=)
PCDHA5 NM_018908.2 -?/. - c.2352+52048G>A r.(=) p.(=)
PCDHA6 NM_018909.2 -?/. - c.2394+45690G>A r.(=) p.(=)
PCDHA7 NM_018910.2 -?/. - c.2355+39437G>A r.(=) p.(=)
PCDHA8 NM_018911.2 -?/. - c.2394+32460G>A r.(=) p.(=)
PCDHA9 NM_031857.1 -?/. - c.2394+25286G>A r.(=) p.(=)


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