Variant #0001035996 (NC_000007.13:g.100491451G>C, NM_001015072.3:c.-4559C>G (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.100491451G>C
DNA change (hg38) -
Published as ACHE(NM_000665.5):c.403C>G (p.P135A)
ISCN -
DB-ID ACHE_000006
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) 0.00102 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 2025-05-05 21:14:00 +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     
UFSP1 NM_001015072.3 -?/. - c.-4559C>G r.(?) p.(=)
ACHE NM_015831.2 -?/. - c.403C>G r.(?) p.(Pro135Ala)


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