Variant #0000609284 (NC_000004.11:g.71508402_71508403insAG, NM_031889.2:c.1259_1260insAG (ENAM))

Chromosome 4
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.71508402_71508403insAG
DNA change (hg38) g.70642685_70642686insAG
Published as ENAM(NM_031889.3):c.1259_1260insAG (p.P422Vfs*27)
ISCN -
DB-ID ENAM_000008 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) 0.00029 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-06-16 13:14:01 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ENAM NM_031889.2 +/. - c.1259_1260insAG r.(?) p.(Pro422ValfsTer27)


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