Variant #0000556876 (NC_000016.9:g.15931819G>A, NM_001040113.1:c.291C>T (MYH11))

Chromosome 16
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.15931819G>A
DNA change (hg38) g.15837962G>A
Published as MYH11(NM_001040113.1):c.291C>T (p.N97=), MYH11(NM_001040113.2):c.291C>T (p.N97=), MYH11(NM_002474.3):c.291C>T (p.N97=)
ISCN -
DB-ID MYH11_000131 See all 3 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) 0.00182 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYH11 NM_001040113.1 -/. - c.291C>T r.(?) p.(Asn97=)
MYH11 NM_002474.2 -/. - c.291C>T r.(?) p.(Asn97=)
NDE1 NM_017668.2 -/. - c.*113711G>A r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.