Variant #0000809519 (NC_000022.10:g.26239784C>A, NM_032608.5:c.3291C>A (MYO18B))

Chromosome 22
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.26239784C>A
DNA change (hg38) -
Published as MYO18B(NM_001318245.1):c.3294C>A (p.(Asp1098Glu)), MYO18B(NM_032608.7):c.3291C>A (p.D1097E)
ISCN -
DB-ID MYO18B_000031 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) 0.00237 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYO18B NM_032608.5 ?/. - c.3291C>A r.(?) p.(Asp1097Glu)


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