Variant #0000865703 (NC_000018.9:g.46645115A>C, NM_017653.3:c.1745T>G (DYM))

Chromosome 18
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.46645115A>C
DNA change (hg38) -
Published as DYM(NM_017653.3):c.1745T>G (p.(Leu582Arg))
ISCN -
DB-ID DYM_000033
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) 1.0E-5 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 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DYM NM_001353214.3 ?/. - c.1910T>G r.(?) p.(Leu637Arg)
DYM NM_017653.3 ?/. - c.1745T>G r.(?) p.(Leu582Arg)


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