Variant #0000863063 (NC_000012.11:g.56082682dup, NM_002206.2:c.2905dup (ITGA7))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.56082682dup
DNA change (hg38) -
Published as ITGA7(NM_002206.2):c.2905dup (p.(Arg969ProfsTer153))
ISCN -
DB-ID BLOC1S1_000026
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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BLOC1S1 NM_001487.3 +?/. - c.-27154dup r.(?) p.(=)
ITGA7 NM_002206.2 +?/. - c.2905dup r.(?) p.(Arg969ProfsTer153)
METTL7B NM_152637.2 +?/. - c.*4849dup r.(?) p.(=)


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