Variant #0000524496 (NC_000005.9:g.140262850C>G, NC_000005.9(NM_018900.2):c.2394+94581C>G (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.140262850C>G
DNA change (hg38) -
Published as PCDHA13(NM_018904.3):c.997C>G (p.H333D)
ISCN -
DB-ID PCDHA1_000056
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) 7.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PCDHAC1 NM_018898.3 ?/. - c.-43628C>G r.(?) p.(=)
PCDHAC2 NM_018899.5 ?/. - c.-83502C>G r.(?) p.(=)
PCDHA1 NM_018900.2 ?/. - c.2394+94581C>G r.(=) p.(=)
PCDHA10 NM_018901.2 ?/. - c.2388+24829C>G r.(=) p.(=)
PCDHA11 NM_018902.3 ?/. - c.2391+11771C>G r.(=) p.(=)
PCDHA12 NM_018903.2 ?/. - c.2367+5426C>G r.(=) p.(=)
PCDHA13 NM_018904.2 ?/. - c.997C>G r.(?) p.(His333Asp)
PCDHA2 NM_018905.2 ?/. - c.2388+85913C>G r.(=) p.(=)
PCDHA3 NM_018906.2 ?/. - c.2394+79674C>G r.(=) p.(=)
PCDHA4 NM_018907.2 ?/. - c.2385+73693C>G r.(=) p.(=)
PCDHA5 NM_018908.2 ?/. - c.2352+59138C>G r.(=) p.(=)
PCDHA6 NM_018909.2 ?/. - c.2394+52780C>G r.(=) p.(=)
PCDHA7 NM_018910.2 ?/. - c.2355+46527C>G r.(=) p.(=)
PCDHA8 NM_018911.2 ?/. - c.2394+39550C>G r.(=) p.(=)
PCDHA9 NM_031857.1 ?/. - c.2394+32376C>G r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.