Variant #0000531303 (NC_000007.13:g.150745974T>C, NM_004935.3:c.*5122A>G (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.150745974T>C
DNA change (hg38) g.151048887T>C
Published as ASIC3(NM_020321.3):c.2T>C (p.M1?)
ISCN -
DB-ID ABCB8_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) 7.0E-5 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-23 15:00:25 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ASIC3 NM_004769.3 ?/. - c.2T>C r.(?) p.(Met1?)
CDK5 NM_004935.3 ?/. - c.*5122A>G r.(=) p.(=)
ABCB8 NM_007188.3 ?/. - c.*3538T>C r.(=) p.(=)


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