Variant #0000951074 (NC_000017.10:g.79990655C>G, NM_005052.2:c.176C>G (RAC3))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.79990655C>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID RAC3_000001 See all 2 reported entries
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RAC3 NM_005052.2 +/. - c.176C>G r.(?) p.(Ala59Gly)
DCXR NM_016286.3 +/. - c.*3181G>C r.(=) p.(=)
LRRC45 NM_144999.2 +/. - c.*1974C>G r.(=) p.(=)


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