Variant #0000560496 (NC_000017.10:g.17697129_17697134del, NM_030665.3:c.867_872del (RAI1))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.17697129_17697134del
DNA change (hg38) g.17793815_17793820del
Published as RAI1(NM_030665.3):c.838_843del (p.(Gln282_Gln283del)), RAI1(NM_030665.3):c.867_872delGCAGCA (p.Q290_Q291del), RAI1(NM_030665.4):c.867_872delGCAGCA ...
ISCN -
DB-ID RAI1_000021 See all 4 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) Retrieve
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 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SREBF1 NM_004176.4 -/. - c.*18837_*18842del r.(=) p.(=)
RAI1 NM_030665.3 -/. - c.867_872del r.(?) p.(Gln290_Gln291del)


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