Variant #0000719553 (NC_000003.11:g.52825548_52825549insTAGAAGTTTCTGA, NM_002217.3:c.-3272_-3271insTAGAAGTTTCTGA (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.52825548_52825549insTAGAAGTTTCTGA
DNA change (hg38) -
Published as ITIH1(NM_002215.3):c.2510_2511insTAGAAGTTTCTGA (p.I838Rfs*4)
ISCN -
DB-ID ITIH1_000003
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) 0 View details
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.2510_2511insTAGAAGTTTCTGA r.(?) p.(Ile838Argfs*4)
ITIH3 NM_002217.3 ?/. - c.-3272_-3271insTAGAAGTTTCTGA r.(?) p.(=)


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