Variant #0001053543 (NC_000010.10:g.50819807G>C, NM_020549.4:c.-2429G>C (CHAT))

Chromosome 10
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.50819807G>C
DNA change (hg38) -
Published as SLC18A3(NM_003055.3):c.1021G>C (p.(Gly341Arg))
ISCN -
DB-ID CHAT_000089
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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC18A3 NM_003055.2 ?/. - c.1021G>C r.(?) p.(Gly341Arg)
CHAT NM_020549.4 ?/. - c.-2429G>C r.(?) p.(=)


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