Variant #0000991257 (NC_000001.10:g.39896387A>C, NM_015038.1:c.*16166A>C (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.39896387A>C
DNA change (hg38) -
Published as MACF1(NM_012090.5):c.10958A>C (p.(Glu3653Ala))
ISCN -
DB-ID KIAA0754_000165
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) 5.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:07:21 +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     
MACF1 NM_001394062.1 -?/. - c.17144A>C r.(?) p.(Glu5715Ala)
KIAA0754 NM_015038.1 -?/. - c.*16166A>C r.(=) p.(=)


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