Variant #0000252215 (NC_000012.11:g.56081971A>G, NC_000012.11(NM_002206.2):c.3057+15T>C (ITGA7))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.56081971A>G
DNA change (hg38) g.55688187A>G
Published as ITGA7(NM_001144996.2):c.3069+15T>C
ISCN -
DB-ID ITGA7_010003
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) 6.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BLOC1S1 NM_001487.3 -?/. - c.-27865A>G r.(?) p.(=)
ITGA7 NM_002206.2 -?/. - c.3057+15T>C r.(=) p.(=)
METTL7B NM_152637.2 -?/. - c.*4138A>G r.(=) p.(=)


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