Variant #0000951073 (NC_000017.10:g.79987415G>C, NM_005052.2:c.-2223G>C (RAC3))

Chromosome 17
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.79987415G>C
DNA change (hg38) -
Published as LRRC45(NM_144999.2):c.1402-4G>C (p.?)
ISCN -
DB-ID RAC3_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) 0.01655 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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.-2223G>C r.(?) p.(=)
LRRC45 NM_144999.2 -?/. - c.1402-4G>C r.spl? p.?


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