Variant #0000514437 (NC_000002.11:g.212578393dup, NC_000002.11(NM_005235.2):c.884-7dup (ERBB4))

Chromosome 2
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.212578393dup
DNA change (hg38) g.211713668dup
Published as ERBB4(NM_005235.2):c.884-7_884-6insT, ERBB4(NM_005235.3):c.884-7_884-6insT, ERBB4(NM_005235.3):c.884-8dupT
ISCN -
DB-ID ERBB4_000047 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERBB4 NM_005235.2 -/. - c.884-7dup r.(=) p.(=)


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