Variant #0000568174 (NC_000019.9:g.50813043_50813047del, NM_024729.3:c.5984_5988del (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.50813043_50813047del
DNA change (hg38) g.50309786_50309790del
Published as MYH14(NM_001077186.1):c.6008_6012del (p.(Gln2003delinsProLeuProCysProGlnMetHis)), MYH14(NM_001145809.1):c.6107_6111delAGTGA (p.Q2036Pfs*9)
ISCN -
DB-ID MYH14_000151 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 11:08:33 +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.6107_6111del r.(?) p.(Gln2036ProfsTer9)
KCNC3 NM_004977.2 -?/. - c.*6325_*6329del r.(=) p.(=)
MYH14 NM_024729.3 -?/. - c.5984_5988del r.(?) p.(Gln1995ProfsTer9)


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