Variant #0000560473 (NC_000017.10:g.17696546C>T, NM_030665.3:c.284C>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.17696546C>T
DNA change (hg38) g.17793232C>T
Published as RAI1(NM_030665.3):c.284C>T (p.P95L), RAI1(NM_030665.4):c.284C>T (p.P95L)
ISCN -
DB-ID RAI1_000089 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) 0.0001 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-10-29 21:08:56 +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.*19390G>A r.(=) p.(=)
RAI1 NM_030665.3 ?/. - c.284C>T r.(?) p.(Pro95Leu)


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