Variant #0000551289 (NC_000014.8:g.103396618G>A, NM_006035.3:c.*3431C>T (CDC42BPB))

Chromosome 14
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.103396618G>A
DNA change (hg38) g.102930281G>A
Published as AMN(NM_030943.3):c.1123G>A (p.(Val375Ile))
ISCN -
DB-ID AMN_000027
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CDC42BPB NM_006035.3 -?/. - c.*3431C>T r.(=) p.(=)
AMN NM_030943.3 -?/. - c.1123G>A r.(?) p.(Val375Ile)


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