Variant #0000325236 (NC_000017.10:g.17697123_17697134dup, NM_030665.3:c.861_872dup (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.17697123_17697134dup
DNA change (hg38) g.17793809_17793820dup
Published as RAI1(NM_030665.3):c.831_832insCAGCAGCAGCAG (p.(Asp277_Gln278insGlnGlnGlnGln)), RAI1(NM_030665.4):c.861_872dupGCAGCAGCAGCA (p.Q288_Q291dup)
ISCN -
DB-ID RAI1_000017 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) Retrieve
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 2022-11-01 13:01:21 +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.*18831_*18842dup r.(=) p.(=)
RAI1 NM_030665.3 ?/. - c.861_872dup r.(?) p.(Gln288_Gln291dup)


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