Variant #0000722313 (NC_000009.11:g.134381543G>C, NM_007171.3:c.165G>C (POMT1))

Chromosome 9
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.134381543G>C
DNA change (hg38) -
Published as POMT1(NM_001353198.1):c.3G>C (p.M1?)
ISCN -
DB-ID UCK1_000029
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POMT1 NM_007171.3 ?/. - c.165G>C r.(?) p.(Met55Ile)
UCK1 NM_031432.2 ?/. - c.*18884C>G r.(=) p.(=)


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