Variant #0000560487 (NC_000017.10:g.17697102del, NM_030665.3:c.840del (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.17697102del
DNA change (hg38) g.17793788del
Published as RAI1(NM_030665.3):c.840del (p.(Gln280HisfsTer84)), RAI1(NM_030665.3):c.840delG (p.Q280Hfs*84), RAI1(NM_030665.4):c.840_843delGCAGinsCAG (p.Q280Hfs...)
ISCN -
DB-ID RAI1_000033 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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +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.*18834del r.(?) p.(=)
RAI1 NM_030665.3 -/. - c.840del r.(?) p.(Gln280HisfsTer84)


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