Variant #0000296251 (NC_000010.10:g.75397587C>G, NM_021245.3:c.167G>C (MYOZ1))

Chromosome 10
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.75397587C>G
DNA change (hg38) g.73637829C>G
Published as MYOZ1(NM_021245.3):c.167G>C (p.G56A), MYOZ1(NM_021245.4):c.167G>C (p.G56A)
ISCN -
DB-ID MYOZ1_000011 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) 0.00017 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYOZ1 NM_021245.3 ?/. - c.167G>C r.(?) p.(Gly56Ala)


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