Variant #0000325270 (NC_000017.10:g.17707127C>T, NM_030665.3:c.5623C>T (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.17707127C>T
DNA change (hg38) g.17803813C>T
Published as RAI1(NM_030665.3):c.5623C>T (p.(Leu1875Phe))
ISCN -
DB-ID RAI1_000073
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SREBF1 NM_004176.4 ?/. - c.*8809G>A r.(=) p.(=)
RAI1 NM_030665.3 ?/. - c.5623C>T r.(?) p.(Leu1875Phe)


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