Variant #0000347882 (NC_000009.11:g.131010965T>C, NM_004408.2:c.2009T>C (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.131010965T>C
DNA change (hg38) g.128248686T>C
Published as -
ISCN -
DB-ID DNM1_000011
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNM1 NM_001288739.1 ?/. - c.2009T>C r.(?) p.(Met670Thr)
DNM1 NM_004408.2 ?/. - c.2009T>C r.(?) p.(Met670Thr)
CIZ1 NM_012127.2 ?/. - c.-44506A>G r.(?) p.(=)


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