Variant #0001003846 (NC_000017.10:g.79990880G>A, NM_005052.2:c.283G>A (RAC3))

Chromosome 17
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.79990880G>A
DNA change (hg38) -
Published as RAC3(NM_005052.2):c.283G>A (p.(Ala95Thr))
ISCN -
DB-ID DCXR_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) 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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RAC3 NM_005052.2 ?/. - c.283G>A r.(?) p.(Ala95Thr)
DCXR NM_016286.3 ?/. - c.*2956C>T r.(=) p.(=)
LRRC45 NM_144999.2 ?/. - c.*2199G>A r.(=) p.(=)


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