Variant #0000997510 (NC_000009.11:g.131012518C>T, NM_004408.2:c.2201C>T (DNM1))

Chromosome 9
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.131012518C>T
DNA change (hg38) -
Published as DNM1(NM_004408.2):c.2201C>T (p.(Ala734Val))
ISCN -
DB-ID CIZ1_000067
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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNM1 NM_001288739.1 ?/. - c.2201C>T r.(?) p.(Ala734Val)
DNM1 NM_004408.2 ?/. - c.2201C>T r.(?) p.(Ala734Val)
CIZ1 NM_012127.2 ?/. - c.-46059G>A r.(?) p.(=)


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