Variant #0000331964 (NC_000007.13:g.150746339G>A, NM_004935.3:c.*4757C>T (CDK5))

Chromosome 7
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.150746339G>A
DNA change (hg38) g.151049252G>A
Published as ASIC3(NM_004769.3):c.367G>A (p.(Ala123Thr))
ISCN -
DB-ID ASIC3_000001
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) 0.0015 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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ASIC3 NM_004769.3 ?/. - c.367G>A r.(?) p.(Ala123Thr)
CDK5 NM_004935.3 ?/. - c.*4757C>T r.(=) p.(=)
ABCB8 NM_007188.3 ?/. - c.*3903G>A r.(=) p.(=)


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