Variant #0000607503 (NC_000002.11:g.219924908_219924910del, NM_002181.3:c.283_285del (IHH))

Chromosome 2
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.219924908_219924910del
DNA change (hg38) g.219060186_219060188del
Published as IHH(NM_002181.3):c.283_285del (p.(Glu95del)), IHH(NM_002181.3):c.283_285delGAG (p.E95del)
ISCN -
DB-ID IHH_000008 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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2021-02-08 18:36:18 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IHH NM_002181.3 +/. - c.283_285del r.(?) p.(Glu95del)


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