Variant #0000568168 (NC_000019.9:g.50813032_50813033del, NM_024729.3:c.5973_5974del (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.50813032_50813033del
DNA change (hg38) g.50309775_50309776del
Published as MYH14(NM_001077186.1):c.5997_5998del (p.(Ala2000ProfsTer13)), MYH14(NM_001145809.1):c.6096_6097delAG (p.A2033Pfs*13)
ISCN -
DB-ID MYH14_000148 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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-16 11:08:14 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYH14 NM_001145809.1 -?/. - c.6096_6097del r.(?) p.(Ala2033ProfsTer13)
KCNC3 NM_004977.2 -?/. - c.*6339_*6340del r.(=) p.(=)
MYH14 NM_024729.3 -?/. - c.5973_5974del r.(?) p.(Ala1992ProfsTer13)


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