Variant #0000895625 (NC_000022.10:g.26423285C>T, NM_032608.5:c.7345C>T (MYO18B))

Chromosome 22
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.26423285C>T
DNA change (hg38) -
Published as MYO18B(NM_001318245.1):c.7348C>T (p.R2450W), MYO18B(NM_032608.7):c.7345C>T (p.R2449W)
ISCN -
DB-ID MYO18B_000020 See all 3 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) 0.00461 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYO18B NM_032608.5 -?/. - c.7345C>T r.(?) p.(Arg2449Trp)


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