Variant #0001016255 (NC_000020.10:g.30419532G>A, NM_033118.3:c.1451G>A (MYLK2))

Chromosome 20
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.30419532G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID MYLK2_000071
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs781515957
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-10-30 14:25:02 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYLK2 NM_033118.3 ?/. - c.1451G>A r.(?) p.(Gly484Glu)


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