Variant #0000997503 (NC_000009.11:g.130980572A>G, NM_004408.2:c.224A>G (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.130980572A>G
DNA change (hg38) -
Published as DNM1(NM_004408.4):c.224A>G (p.N75S)
ISCN -
DB-ID CIZ1_000060
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) 4.0E-5 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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNM1 NM_001288739.1 -?/. - c.224A>G r.(?) p.(Asn75Ser)
DNM1 NM_004408.2 -?/. - c.224A>G r.(?) p.(Asn75Ser)
CIZ1 NM_012127.2 -?/. - c.-14113T>C r.(?) p.(=)


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