Variant #0001031287 (NC_000001.10:g.153603057G>A, NM_015607.3:c.-3780G>A (CHTOP))

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.153603057G>A
DNA change (hg38) -
Published as S100A1(NM_006271.2):c.60G>A (p.(Ser20=))
ISCN -
DB-ID CHTOP_000003
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) 0.00035 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 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     
S100A13 NM_005979.2 ?/. - c.-2638C>T r.(?) p.(=)
S100A1 NM_006271.1 ?/. - c.60G>A r.(?) p.(=)
CHTOP NM_015607.3 ?/. - c.-3780G>A r.(?) p.(=)


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