Variant #0000332821 (NC_000009.11:g.134379683G>A, NM_007171.3:c.78G>A (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.134379683G>A
DNA change (hg38) g.131504296G>A
Published as POMT1(NM_001077365.1):c.78G>A (p.(Gly26=))
ISCN -
DB-ID POMT1_000096 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) 0.00244 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-05-09 15:51:19 +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.78G>A r.(?) p.(Gly26=)
PRRC2B NM_013318.3 -?/. - c.*8422G>A r.(=) p.(=)
UCK1 NM_031432.2 -?/. - c.*20744C>T r.(=) p.(=)


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