Variant #0000890695 (NC_000012.11:g.56101438dup, NM_002206.2:c.34dup (ITGA7))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.56101438dup
DNA change (hg38) -
Published as ITGA7(NM_001144996.1):c.34dup (p.(Ala12Glyfs*91))
ISCN -
DB-ID BLOC1S1_000032
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-11-01 13:01:21 +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.-8398dup r.(?) p.(=)
ITGA7 NM_002206.2 +?/. - c.34dup r.(?) p.(Ala12Glyfs*91)
METTL7B NM_152637.2 +?/. - c.*23605dup r.(?) p.(=)


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