Variant #0000913900 (NC_000012.11:g.56094948G>A, NC_000012.11(NM_002206.2):c.415-10C>T (ITGA7))

Chromosome 12
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.56094948G>A
DNA change (hg38) -
Published as ITGA7(NM_002206.3):c.415-10C>T
ISCN -
DB-ID ITGA7_000022 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) 0.0628 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 2023-01-11 15:44:22 +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.-14888G>A r.(?) p.(=)
ITGA7 NM_002206.2 -/. - c.415-10C>T r.(=) p.(=)
METTL7B NM_152637.2 -/. - c.*17115G>A r.(=) p.(=)


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