Variant #0000504228 (NC_000001.10:g.171605095_171605102del, NM_000261.1:c.1480_1487del (MYOC))

Chromosome 1
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.171605095_171605102del
DNA change (hg38) g.171635955_171635962del
Published as MYOC(NM_000261.1):c.1480_1487del (p.(Met494LeufsTer2))
ISCN -
DB-ID MYOC_000098
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_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 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYOC NM_000261.1 ?/. - c.1480_1487del r.(?) p.(Met494LeufsTer2)


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