Variant #0001032080 (NC_000001.10:g.44466729T>A, NC_000001.10(NM_201649.3):c.1555-2A>T (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.44466729T>A
DNA change (hg38) -
Published as SLC6A9(NM_001024845.3):c.1336-2A>T
ISCN -
DB-ID CCDC24_000009
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) Retrieve
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.*4897T>A r.(=) p.(=)
SLC6A9 NM_201649.3 ?/. - c.1555-2A>T r.spl? p.?


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