Variant #0001065765 (NC_000012.11:g.56091754T>C, NM_002206.2:c.1249A>G (ITGA7))

Chromosome 12
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.56091754T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID BLOC1S1_000061
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) 0.00013 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BLOC1S1 NM_001487.3 ?/. - c.-18082T>C r.(?) p.(=)
ITGA7 NM_002206.2 ?/. - c.1249A>G r.(?) p.(Ser417Gly)
METTL7B NM_152637.2 ?/. - c.*13921T>C r.(=) p.(=)


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