Variant #0000949996 (NC_000012.11:g.56101421A>C, NM_002206.2:c.46T>G (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.56101421A>C
DNA change (hg38) -
Published as ITGA7(NM_002206.2):c.46T>G (p.(Cys16Gly)), ITGA7(NM_002206.3):c.46T>G (p.C16G)
ISCN -
DB-ID BLOC1S1_000044 See all 2 reported entries
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) 0.00142 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 2023-11-27 17:35:39 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BLOC1S1 NM_001487.3 -?/. - c.-8415A>C r.(?) p.(=)
ITGA7 NM_002206.2 -?/. - c.46T>G r.(?) p.(Cys16Gly)
METTL7B NM_152637.2 -?/. - c.*23588A>C r.(=) p.(=)


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