Variant #0000266820 (NC_000009.11:g.130941121T>C, NM_004408.2:c.-24629T>C (DNM1))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.130941121T>C
DNA change (hg38) g.128178842T>C
Published as CIZ1(NM_001257975.2):c.1455A>G (p.V485=)
ISCN -
DB-ID CIZ1_000004
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) 0.00765 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +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.-24629T>C r.(?) p.(=)
DNM1 NM_004408.2 -?/. - c.-24629T>C r.(?) p.(=)
CIZ1 NM_012127.2 -?/. - c.1365A>G r.(?) p.(Val455=)


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