Variant #0000324612 (NC_000016.9:g.15785124C>G, NM_001040113.1:c.*12865G>C (MYH11))

Chromosome 16
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.15785124C>G
DNA change (hg38) g.15691267C>G
Published as NDE1(NM_001143979.1):c.647C>G (p.(Pro216Arg))
ISCN -
DB-ID NDE1_000010
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYH11 NM_001040113.1 ?/. - c.*12865G>C r.(=) p.(=)
MYH11 NM_002474.2 ?/. - c.*12724G>C r.(=) p.(=)
NDE1 NM_017668.2 ?/. - c.647C>G r.(?) p.(Pro216Arg)


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