Variant #0000548661 (NC_000012.11:g.56090984G>C, NC_000012.11(NM_002206.2):c.1567+16C>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.56090984G>C
DNA change (hg38) g.55697200G>C
Published as ITGA7(NM_001144996.1):c.1579+16C>G (p.(=))
ISCN -
DB-ID ITGA7_000029 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) 0.00027 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 2019-07-18 18:22:55 +02:00 (CEST)
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.-18852G>C r.(?) p.(=)
ITGA7 NM_002206.2 -?/. - c.1567+16C>G r.(=) p.(=)
METTL7B NM_152637.2 -?/. - c.*13151G>C r.(=) p.(=)


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