Variant #0000536639 (NC_000009.11:g.134398483G>A, NM_007171.3:c.2234G>A (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.134398483G>A
DNA change (hg38) g.131523096G>A
Published as POMT1(NM_001077365.1):c.2168G>A (p.(Arg723Gln)), POMT1(NM_007171.3):c.2234G>A (p.R745Q)
ISCN -
DB-ID POMT1_000097 See all 3 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) 0.00045 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 2023-04-16 21:50:28 +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.2234G>A r.(?) p.(Arg745Gln)
UCK1 NM_031432.2 ?/. - c.*1944C>T r.(=) p.(=)


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