Variant #0000530069 (NC_000007.13:g.100486464T>G, NM_001015072.3:c.429A>C (UFSP1))

Chromosome 7
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.100486464T>G
DNA change (hg38) g.100888843T>G
Published as UFSP1(NM_001015072.3):c.429A>C (p.(Ter143Cysext*?))
ISCN -
DB-ID ACHE_000001
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) 0.00094 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
UFSP1 NM_001015072.3 -?/. - c.429A>C r.(?) p.(Ter143CysextTer?)
ACHE NM_015831.2 -?/. - c.*2115A>C r.(=) p.(=)
SRRT NM_015908.5 -?/. - c.*294T>G r.(=) p.(=)


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