Variant #0000266822 (NC_000009.11:g.130931672G>A, NM_004408.2:c.-34078G>A (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.130931672G>A
DNA change (hg38) g.128169393G>A
Published as CIZ1(NM_001257975.2):c.2313+13C>T
ISCN -
DB-ID CIZ1_000002
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) 0.00252 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.-34078G>A r.(?) p.(=)
DNM1 NM_004408.2 -?/. - c.-34078G>A r.(?) p.(=)
CIZ1 NM_012127.2 -?/. - c.2145+13C>T r.(=) p.(=)


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