Variant #0000352001 (NC_000009.11:g.134382673C>T, NC_000009.11(NM_007171.3):c.281-82C>T (POMT1))

Chromosome 9
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.134382673C>T
DNA change (hg38) g.131507286C>T
Published as -
ISCN -
DB-ID POMT1_000053
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs6597501
Origin Germline
Segregation -
Frequency -
Re-site -HhI
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2006-09-15 20:05:00 +02:00 (CEST)
Date last edited 2012-11-02 20:43:02 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POMT1 NM_007171.3 -/. 5 c.281-82C>T r.(?) p.(=)


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