Variant #0000560522 (NC_000017.10:g.17700099del, NM_030665.3:c.3837del (RAI1))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.17700099del
DNA change (hg38) g.17796785del
Published as RAI1(NM_030665.3):c.3837delC (p.K1280Sfs*35)
ISCN -
DB-ID RAI1_000116
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 2020-07-13 10:41:32 +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.*15838del r.(?) p.(=)
RAI1 NM_030665.3 +?/. - c.3837del r.(?) p.(Lys1280SerfsTer35)


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