Variant #0000719554 (NC_000003.11:g.52825552_52825553insCACCC, NM_002217.3:c.-3268_-3267insCACCC (ITIH3))

Chromosome 3
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.52825552_52825553insCACCC
DNA change (hg38) -
Published as ITIH1(NM_002215.3):c.2514_2515insCACCC (p.G839Hfs*24)
ISCN -
DB-ID ITIH1_000004
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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ITIH1 NM_002215.3 ?/. - c.2514_2515insCACCC r.(?) p.(Gly839Hisfs*24)
ITIH3 NM_002217.3 ?/. - c.-3268_-3267insCACCC r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.