Variant #0000132260 (NC_000012.11:g.53823329C>T, NM_020547.2:c.1060C>T (AMHR2))

Chromosome 12
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.53823329C>T
DNA change (hg38) g.53429545C>T
Published as L354F
ISCN -
DB-ID AMHR2_000003 See all 2 reported entries
Variant remarks cDNA expression cloning, near normal activation ID3/SMAD6 transcription
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 13:35:21 +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 -/. 8 c.1060C>T r.(?) p.(Leu354Phe)


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