Variant #0000301140 (NC_000009.11:g.134381495T>C, NC_000009.11(NM_007171.3):c.123-6T>C (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.134381495T>C
DNA change (hg38) g.131506108T>C
Published as POMT1(NM_001136113.2):c.123-6T>C
ISCN -
DB-ID POMT1_000150
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) 7.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.123-6T>C r.(=) p.(=)
UCK1 NM_031432.2 -?/. - c.*18932A>G r.(=) p.(=)


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