Variant #0000256367 (NC_000023.10:g.41555485A>G, NC_000023.10(NM_003688.3):c.430-24702T>C (CASK))

Chromosome X
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.41555485A>G
DNA change (hg38) g.41696232A>G
Published as GPR34(NM_001097579.2):c.599A>G (p.N200S)
ISCN -
DB-ID CASK_000044
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) 4.0E-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 2018-01-15 20:58:59 +01:00 (CET)
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.430-24702T>C r.(=) p.(=)
GPR34 NM_005300.3 ?/. - c.599A>G r.(?) p.(Asn200Ser)
GPR82 NM_080817.4 ?/. - c.-28163A>G r.(?) p.(=)


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