Variant #0001036197 (NC_000007.13:g.150749682C>T, NM_004935.3:c.*1414G>A (CDK5))

Chromosome 7
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.150749682C>T
DNA change (hg38) -
Published as ASIC3(NM_020321.3):c.1559C>T (p.(Pro520Leu))
ISCN -
DB-ID ABCB8_000006
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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ASIC3 NM_004769.3 -?/. - c.1539C>T r.(?) p.(=)
CDK5 NM_004935.3 -?/. - c.*1414G>A r.(=) p.(=)
ABCB8 NM_007188.3 -?/. - c.*7246C>T r.(=) p.(=)


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