Variant #0000980377 (NC_000012.11:g.56088579G>A, NM_002206.2:c.2179C>T (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.56088579G>A
DNA change (hg38) -
Published as ITGA7(NM_002206.3):c.2179C>T (p.(Arg727Trp))
ISCN -
DB-ID BLOC1S1_000048
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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
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.-21257G>A r.(?) p.(=)
ITGA7 NM_002206.2 ?/. - c.2179C>T r.(?) p.(Arg727Trp)
METTL7B NM_152637.2 ?/. - c.*10746G>A r.(=) p.(=)


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