Variant #0000989357 (NC_000017.10:g.10312775T>C, NM_002472.2:c.1718A>G (MYH8))

Chromosome 17
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.10312775T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID MYH8_000052
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs754437166
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 4.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-08-03 16:51:01 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYH8 NM_002472.2 ?/. - c.1718A>G r.(?) p.(Lys573Arg)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.