Variant #0000132261 (NC_000012.11:g.53819477T>A, NM_020547.2:c.626T>A (AMHR2))

Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.53819477T>A
DNA change (hg38) g.53425693T>A
Published as I209N
ISCN -
DB-ID AMHR2_000002 See all 2 reported entries
Variant remarks cDNA expression cloning, absent activation ID3/SMAD6 transcription (dominant negative effect)
Reference PubMed: Li 2016, Journal: Li 2016
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2016-10-14 13:38:50 +02:00 (CEST)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AMHR2 NM_020547.2 +/. 6 c.626T>A r.(?) p.(Ile209Asn)


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