Variant #0000565288 (NC_000018.9:g.67863852_67863854dup, NM_173630.3:c.725_727dup (RTTN))

Chromosome 18
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.67863852_67863854dup
DNA change (hg38) g.70196616_70196618dup
Published as RTTN(NM_173630.3):c.725_727dupGAG (p.G242dup), RTTN(NM_173630.4):c.723_725dupGAG (p.G242dup)
ISCN -
DB-ID RTTN_000118 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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RTTN NM_173630.3 -/. - c.725_727dup r.(?) p.(Gly242dup)


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