Variant #0000947251 (NC_000001.10:g.39920726C>T, NM_015038.1:c.*40505C>T (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.39920726C>T
DNA change (hg38) -
Published as MACF1(NM_012090.5):c.14855C>T (p.P4952L)
ISCN -
DB-ID KIAA0754_000121
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) 0.0003 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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MACF1 NM_001394062.1 -?/. - c.21032C>T r.(?) p.(Pro7011Leu)
KIAA0754 NM_015038.1 -?/. - c.*40505C>T r.(=) p.(=)


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