Variant #0000622185 (NC_000009.11:g.134394274C>T, NM_007171.3:c.1482C>T (POMT1))

Chromosome 9
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.134394274C>T
DNA change (hg38) g.131518887C>T
Published as POMT1(NM_001353198.1):c.1320C>T (p.V440=)
ISCN -
DB-ID UCK1_000022
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) 0.00052 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2020-06-26 10:34:27 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POMT1 NM_007171.3 -?/. - c.1482C>T r.(?) p.(Val494=)
UCK1 NM_031432.2 -?/. - c.*6153G>A r.(=) p.(=)


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