Variant #0000096445 (NC_000023.10:g.113818520=, NM_001256760.1:c.-850C= (HTR2C))

Chromosome X
Allele Parent #1
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.113818520=
DNA change (hg38) g.114584047=
Published as C-759T (NM_000868.3)
ISCN -
DB-ID HTR2C_000000 See all 3 reported entries
Variant remarks reference haplotype HTR2C 2-1-1
Reference Reference haplotype
ClinVar ID -
dbSNP ID rs3813929
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2016-05-09 17:25:47 +02:00 (CEST)
Date last edited 2020-07-21 08:59:14 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
HTR2C NM_001256760.1 ?/. _1 c.-850C= HTR2C 2-1-1 r.(?) p.(=)


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