Variant #0000322905 (NC_000012.11:g.56092610C>T, NM_002206.2:c.882G>A (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.56092610C>T
DNA change (hg38) g.55698826C>T
Published as ITGA7(NM_001144996.1):c.894G>A (p.(Val298=))
ISCN -
DB-ID ITGA7_010016
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) 0.00139 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-05-09 15:51:19 +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.-17226C>T r.(?) p.(=)
ITGA7 NM_002206.2 -?/. - c.882G>A r.(?) p.(Val294=)
METTL7B NM_152637.2 -?/. - c.*14777C>T r.(=) p.(=)


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