Variant #0000722315 (NC_000009.11:g.134381575C>T, NM_007171.3:c.197C>T (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.134381575C>T
DNA change (hg38) -
Published as POMT1(NM_001077365.1):c.197C>T (p.(Pro66Leu)), POMT1(NM_001136113.1):c.197C>T (p.P66L), POMT1(NM_001136113.2):c.197C>T (p.P66L)
ISCN -
DB-ID POMT1_000153 See all 7 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) 5.0E-5 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +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.197C>T r.(?) p.(Pro66Leu)
UCK1 NM_031432.2 ?/. - c.*18852G>A r.(=) p.(=)


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