Variant #0000980376 (NC_000012.11:g.56077691T>C, NM_002206.2:c.*1151A>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.56077691T>C
DNA change (hg38) -
Published as METTL7B(NM_152637.3):c.593T>C (p.(Ile198Thr))
ISCN -
DB-ID BLOC1S1_000047
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) 0.00039 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 2024-04-19 20:27:30 +02:00 (CEST)
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.-32145T>C r.(?) p.(=)
ITGA7 NM_002206.2 -?/. - c.*1151A>G r.(=) p.(=)
METTL7B NM_152637.2 -?/. - c.593T>C r.(?) p.(Ile198Thr)


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