Variant #0000298856 (NC_000004.11:g.41748001_41748015del, NM_003924.3:c.765_779del (PHOX2B))

Chromosome 4
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.41748001_41748015del
DNA change (hg38) g.41745984_41745998del
Published as PHOX2B(NM_003924.4):c.765_779delGGCAGCGGCGGCAGC (p.A256_A260del)
ISCN -
DB-ID PHOX2B_000030 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) 0.00076 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
PHOX2B NM_003924.3 -/. - c.765_779del - r.(?) p.(Ala256_Ala260del)


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