Variant #0000728904 (NC_000023.10:g.41586346A>C, CASK(NM_003688.3):c.429+12291T>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.41586346A>C
DNA change (hg38) -
Published as GPR82(NM_080817.4):c.67A>C (p.I23L)
ISCN -
DB-ID CASK_000136
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CASK NM_003688.3 -?/. - c.429+12291T>G r.(=) p.(=)
GPR34 NM_005300.3 -?/. - c.*30314A>C r.(=) p.(=)
GPR82 NM_080817.4 -?/. - c.67A>C r.(?) p.(Ile23Leu)