Variant #0000305556 (NC_000004.11:g.41748022_41748036del, NM_003924.3:c.741_755del (PHOX2B))

Chromosome 4
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.41748022_41748036del
DNA change (hg38) g.41746005_41746019del
Published as PHOX2B(NM_003924.3):c.741_755delCGCGGCAGCGGCGGC (p.A256_A260del), PHOX2B(NM_003924.4):c.741_755delCGCGGCAGCGGCGGC (p.A256_A260del)
ISCN -
DB-ID PHOX2B_000032 See all 3 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +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.741_755del - r.(?) p.(Ala256_Ala260del)


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