Variant #0000611875 (NC_000009.11:g.130953045_130953047dup, NM_004408.2:c.-12705_-12703dup (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.130953045_130953047dup
DNA change (hg38) g.128190766_128190768dup
Published as CIZ1(NM_001257975.2):c.190_192dupCAG (p.Q64dup)
ISCN -
DB-ID CIZ1_000028
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNM1 NM_001288739.1 ?/. - c.-12705_-12703dup r.(?) p.(=)
DNM1 NM_004408.2 ?/. - c.-12705_-12703dup r.(?) p.(=)
CIZ1 NM_012127.2 ?/. - c.100_102dup r.(?) p.(Gln34dup)


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