Variant #0001053521 (NC_000010.10:g.27826875C>G, NM_001256410.1:c.603C>G (RAB18))

Chromosome 10
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.27826875C>G
DNA change (hg38) -
Published as RAB18(NM_001256411.1):c.449C>G (p.P150R), RAB18(NM_001256411.2):c.449C>G (p.(Pro150Arg))
ISCN -
DB-ID RAB18_000008 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) 1.0E-5 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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RAB18 NM_001256410.1 ?/. - c.603C>G r.(?) p.(Thr201=)


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