Variant #0000863902 (NC_000015.9:g.56735955C>T, NM_018365.2:c.784G>A (MNS1))

Chromosome 15
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.56735955C>T
DNA change (hg38) -
Published as MNS1(NM_018365.3):c.784G>A (p.E262K)
ISCN -
DB-ID MNS1_000008
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MNS1 NM_018365.2 -?/. - c.784G>A r.(?) p.(Glu262Lys)
TEX9 NM_198524.1 -?/. - c.*30-1914C>T r.(=) p.(=)


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