Variant #0001053544 (NC_000010.10:g.50856559G>A, NM_020549.4:c.1288G>A (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.50856559G>A
DNA change (hg38) -
Published as CHAT(NM_001142933.2):c.1042G>A (p.V348M), CHAT(NM_020549.5):c.1288G>A (p.(Val430Met))
ISCN -
DB-ID CHAT_000060 See all 4 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) 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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC18A3 NM_003055.2 ?/. - c.*36174G>A r.(=) p.(=)
CHAT NM_020549.4 ?/. - c.1288G>A r.(?) p.(Val430Met)


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