Variant #0001055887 (NC_000017.10:g.17700695G>A, NM_030665.3:c.4433G>A (RAI1))

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.17700695G>A
DNA change (hg38) -
Published as RAI1(NM_030665.4):c.4433G>A (p.(Arg1478Gln))
ISCN -
DB-ID RAI1_000238
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SREBF1 NM_004176.4 ?/. - c.*15241C>T r.(=) p.(=)
RAI1 NM_030665.3 ?/. - c.4433G>A r.(?) p.(Arg1478Gln)


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