Variant #0001032081 (NC_000001.10:g.44466880C>T, NM_201649.3:c.1510G>A (SLC6A9))

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.44466880C>T
DNA change (hg38) -
Published as SLC6A9(NM_001024845.3):c.1291G>A (p.(Val431Met))
ISCN -
DB-ID CCDC24_000010
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) 2.0E-5 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     
CCDC24 NM_152499.1 ?/. - c.*5048C>T r.(=) p.(=)
SLC6A9 NM_201649.3 ?/. - c.1510G>A r.(?) p.(Val504Met)


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