Variant #0000519967 (NC_000003.11:g.46902491C>A, NC_000003.11(NM_000258.2):c.130-14G>T (MYL3))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.46902491C>A
DNA change (hg38) g.46861001C>A
Published as MYL3(NM_000258.2):c.130-14G>T, MYL3(NM_000258.3):c.130-14G>T
ISCN -
DB-ID MYL3_000067 See all 5 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) 0.00164 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYL3 NM_000258.2 -/. - c.130-14G>T r.(=) p.(=)


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