Variant #0000973934 (NC_000001.10:g.39776667dup, NM_015038.1:c.-99271dup (KIAA0754))

Chromosome 1
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.39776667dup
DNA change (hg38) -
Published as MACF1(NM_012090.5):c.3280dup (p.(Gln1094ProfsTer23))
ISCN -
DB-ID KIAA0754_000124
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:20:39 +02:00 (CEST)
Date last edited 2024-08-28 13:07:21 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MACF1 NM_001394062.1 ?/. - c.3265dup r.(?) p.(Gln1089Profs*23)
KIAA0754 NM_015038.1 ?/. - c.-99271dup r.(?) p.(=)


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