Variant #0000555314 (NC_000015.9:g.72190309A>G, NM_006901.3:c.4535T>C (MYO9A))

Chromosome 15
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.72190309A>G
DNA change (hg38) g.71897968A>G
Published as MYO9A(NM_006901.3):c.4535T>C (p.(Met1512Thr)), MYO9A(NM_006901.4):c.4535T>C (p.M1512T)
ISCN -
DB-ID MYO9A_000008 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) 0.00138 View details
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 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYO9A NM_006901.3 -?/. - c.4535T>C r.(?) p.(Met1512Thr)


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