Variant #0000947249 (NC_000001.10:g.39889792T>G, NM_015038.1:c.*9571T>G (KIAA0754))

Chromosome 1
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.39889792T>G
DNA change (hg38) -
Published as MACF1(NM_012090.5):c.10056T>G (p.D3352E)
ISCN -
DB-ID KIAA0754_000119
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) 0.0004 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 2023-11-27 17:35:39 +01:00 (CET)
Date last edited 2024-08-28 13:07:21 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MACF1 NM_001394062.1 -?/. - c.16242T>G r.(?) p.(Asp5414Glu)
KIAA0754 NM_015038.1 -?/. - c.*9571T>G r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.