Variant #0000536610 (NC_000009.11:g.134381495_134381496dup, NC_000009.11(NM_007171.3):c.123-6_123-5dup (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.134381495_134381496dup
DNA change (hg38) g.131506108_131506109dup
Published as POMT1(NM_001077365.1):c.123-6_123-5dup (p.?), POMT1(NM_001136113.2):c.123-6_123-5dupTT
ISCN -
DB-ID UCK1_000003 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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.123-6_123-5dup r.spl? p.?
UCK1 NM_031432.2 -?/. - c.*18938_*18939dup r.(=) p.(=)


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