Variant #0001043312 (NC_000020.10:g.32005660G>A, NM_003098.2:c.566C>T (SNTA1))

Chromosome 20
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.32005660G>A
DNA change (hg38) -
Published as SNTA1(NM_003098.2):c.566C>T (p.(Ser189Leu), p.S189L), SNTA1(NM_003098.3):c.566C>T (p.S189L)
ISCN -
DB-ID SNTA1_000008 See all 5 reported entries
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) 0.0002 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     
SNTA1 NM_003098.2 -?/. - c.566C>T r.(?) p.(Ser189Leu)


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