Variant #0000678031 (NC_000007.13:g.150749657G>A, NM_004935.3:c.*1439C>T (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.150749657G>A
DNA change (hg38) -
Published as ASIC3(NM_020321.3):c.1534G>A (p.E512K)
ISCN -
DB-ID ABCB8_000004
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) 0.00023 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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +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.1518-4G>A r.spl? p.?
CDK5 NM_004935.3 -?/. - c.*1439C>T r.(=) p.(=)
ABCB8 NM_007188.3 -?/. - c.*7221G>A r.(=) p.(=)


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