Variant #0000330588 (NC_000005.9:g.140358582G>C, NM_018900.2:c.2443G>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.140358582G>C
DNA change (hg38) -
Published as PCDHA1(NM_018900.2):c.2443G>C (p.(Gly815Arg))
ISCN -
DB-ID PCDHA1_000031
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) 2.0E-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 2018-01-15 20:58:59 +01:00 (CET)
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.2482G>C r.(?) p.(Gly828Arg)
PCDHAC2 NM_018899.5 ?/. - c.2614G>C r.(?) p.(Gly872Arg)
PCDHA1 NM_018900.2 ?/. - c.2443G>C r.(?) p.(Gly815Arg)
PCDHA10 NM_018901.2 ?/. - c.2437G>C r.(?) p.(Gly813Arg)
PCDHA11 NM_018902.3 ?/. - c.2440G>C r.(?) p.(Gly814Arg)
PCDHA12 NM_018903.2 ?/. - c.2416G>C r.(?) p.(Gly806Arg)
PCDHA13 NM_018904.2 ?/. - c.2443G>C r.(?) p.(Gly815Arg)
PCDHA2 NM_018905.2 ?/. - c.2437G>C r.(?) p.(Gly813Arg)
PCDHA3 NM_018906.2 ?/. - c.2443G>C r.(?) p.(Gly815Arg)
PCDHA4 NM_018907.2 ?/. - c.2434G>C r.(?) p.(Gly812Arg)
PCDHA5 NM_018908.2 ?/. - c.2401G>C r.(?) p.(Gly801Arg)
PCDHA6 NM_018909.2 ?/. - c.2443G>C r.(?) p.(Gly815Arg)
PCDHA7 NM_018910.2 ?/. - c.2404G>C r.(?) p.(Gly802Arg)
PCDHA8 NM_018911.2 ?/. - c.2443G>C r.(?) p.(Gly815Arg)
PCDHA9 NM_031857.1 ?/. - c.2443G>C r.(?) p.(Gly815Arg)


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