Variant #0000560157 (NC_000017.10:g.10296261G>C, NM_002472.2:c.5350C>G (MYH8))

Chromosome 17
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.10296261G>C
DNA change (hg38) g.10392944G>C
Published as MYH8(NM_002472.2):c.5350C>G (p.(Arg1784Gly)), MYH8(NM_002472.3):c.5350C>G (p.R1784G)
ISCN -
DB-ID MYH8_000018 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) 0.00535 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYH8 NM_002472.2 -?/. - c.5350C>G r.(?) p.(Arg1784Gly)


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