Variant #0000850610 (NC_000004.11:g.41749491G>A, NM_003924.3:c.304C>T (PHOX2B))

Chromosome 4
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.41749491G>A
DNA change (hg38) -
Published as PHOX2B(NM_003924.3):c.304C>T (p.R102C), PHOX2B(NM_003924.4):c.304C>T (p.R102C)
ISCN -
DB-ID PHOX2B_000064 See all 2 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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
PHOX2B NM_003924.3 ?/. - c.304C>T - r.(?) p.(Arg102Cys)


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