Variant #0000576001 (NC_000023.10:g.41555359G>C, CASK(NM_003688.3):c.430-24576C>G)

Chromosome X
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.41555359G>C
DNA change (hg38) g.41696106G>C
Published as GPR34(NM_001097579.1):c.473G>C (p.(Arg158Pro))
ISCN -
DB-ID CASK_000085
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) 1.0E-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 2019-07-18 18:22:55 +02:00 (CEST)
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     
CASK NM_003688.3 -?/. - c.430-24576C>G r.(=) p.(=)
GPR34 NM_005300.3 -?/. - c.473G>C r.(?) p.(Arg158Pro)
GPR82 NM_080817.4 -?/. - c.-28289G>C r.(?) p.(=)