Variant #0000536608 (NC_000009.11:g.134379652A>G, NM_007171.3:c.47A>G (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.134379652A>G
DNA change (hg38) g.131504265A>G
Published as POMT1(NM_001077365.1):c.47A>G (p.(Asn16Ser))
ISCN -
DB-ID UCK1_000002
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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
POMT1 NM_007171.3 -?/. - c.47A>G r.(?) p.(Asn16Ser)
PRRC2B NM_013318.3 -?/. - c.*8391A>G r.(=) p.(=)
UCK1 NM_031432.2 -?/. - c.*20775T>C r.(=) p.(=)


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