Variant #0000553154 (NC_000014.8:g.77786793C>A, NM_013382.5:c.232G>T (POMT2))

Chromosome 14
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.77786793C>A
DNA change (hg38) g.77320450C>A
Published as POMT2(NM_013382.5):c.232G>T (p.E78*)
ISCN -
DB-ID GSTZ1_000002 See all 2 reported entries
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) 1.0E-5 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-05 16:19:59 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POMT2 NM_013382.5 +/. - c.232G>T r.(?) p.(Glu78Ter)
GSTZ1 NM_145870.2 +/. - c.-719C>A r.(?) p.(=)


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