Variant #0000895092 (NC_000019.9:g.50755984G>A, NM_024729.3:c.1895G>A (MYH14))

Chromosome 19
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.50755984G>A
DNA change (hg38) -
Published as MYH14(NM_001145809.1):c.1919G>A (p.R640Q), MYH14(NM_001145809.2):c.1919G>A (p.R640Q)
ISCN -
DB-ID MYH14_000155 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) 0.00065 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-11-01 13:41:49 +01:00 (CET)
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     
MYH14 NM_001145809.1 -?/. - c.1919G>A r.(?) p.(Arg640Gln)
MYH14 NM_024729.3 -?/. - c.1895G>A r.(?) p.(Arg632Gln)


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