Variant #0000612637 (NC_000010.10:g.75399756G>A, NM_021245.3:c.20C>T (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.75399756G>A
DNA change (hg38) g.73639998G>A
Published as MYOZ1(NM_021245.4):c.20C>T (p.P7L)
ISCN -
DB-ID MYOZ1_000028
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) 2.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYOZ1 NM_021245.3 ?/. - c.20C>T r.(?) p.(Pro7Leu)
SYNPO2L NM_024875.3 ?/. - c.*6720C>T r.(=) p.(=)


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