Variant #0000325239 (NC_000017.10:g.17697132_17697134dup, NM_030665.3:c.870_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.17697132_17697134dup
DNA change (hg38) g.17793818_17793820dup
Published as RAI1(NM_030665.3):c.832_834dup (p.?), RAI1(NM_030665.3):c.870_872dupGCA (p.Q291dup), RAI1(NM_030665.4):c.870_872dupGCA (p.Q291dup), RAI1(NM_030665...)
ISCN -
DB-ID RAI1_000020
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 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.*18840_*18842dup r.(=) p.(=)
RAI1 NM_030665.3 ?/. - c.870_872dup r.(?) p.(Gln291dup)


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