Variant #0001002983 (NC_000017.10:g.17696485G>T, NM_030665.3:c.223G>T (RAI1))

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.17696485G>T
DNA change (hg38) -
Published as RAI1(NM_030665.3):c.223G>T (p.(Ala75Ser))
ISCN -
DB-ID RAI1_000205
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) 0.0012 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 2024-08-28 13:16:32 +02:00 (CEST)
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.*19451C>A r.(=) p.(=)
RAI1 NM_030665.3 -?/. - c.223G>T r.(?) p.(Ala75Ser)


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