Variant #0000884708 (NC_000002.11:g.212248660C>A, NM_005235.2:c.3607G>T (ERBB4))

Chromosome 2
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.212248660C>A
DNA change (hg38) -
Published as ERBB4(NM_005235.2):c.3607G>T (p.V1203L), ERBB4(NM_005235.3):c.3607G>T (p.V1203L)
ISCN -
DB-ID ERBB4_000034 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) 0 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERBB4 NM_005235.2 -?/. - c.3607G>T r.(?) p.(Val1203Leu)


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