Variant #0000266757 (NC_000010.10:g.50856652G>A, NM_020549.4:c.1381= (CHAT))

Chromosome 10
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.50856652G>A
DNA change (hg38) g.49648606G>A
Published as CHAT(NM_001142933.2):c.1135G>A (p.V379M)
ISCN -
DB-ID CHAT_000055
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) 0.99148 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC18A3 NM_003055.2 -/. - c.*36267G>A r.(=) p.(=)
CHAT NM_020549.4 -/. - c.1381= r.(=) p.(Met461=)


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