Variant #0000991312 (NC_000001.10:g.44461665G>A, NM_201649.3:c.*1552C>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.44461665G>A
DNA change (hg38) -
Published as CCDC24(NM_152499.1):c.757G>A (p.(Gly253Arg))
ISCN -
DB-ID B4GALT2_000004
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) 3.0E-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 2024-08-28 13:07:21 +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     
B4GALT2 NM_003780.4 ?/. - c.*5545G>A r.(=) p.(=)
CCDC24 NM_152499.1 ?/. - c.757G>A r.(?) p.(Gly253Arg)
SLC6A9 NM_201649.3 ?/. - c.*1552C>T r.(=) p.(=)


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