Variant #0001011769 (NC_000019.9:g.17313001C>T, NM_004145.3:c.4725C>T (MYO9B))

Chromosome 19
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.17313001C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID MYO9B_000019
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1320837956
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-10-16 13:30:02 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYO9B NM_004145.3 -?/. - c.4725C>T r.(?) p.(Asn1575=)


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