View genomic variant #0000000011

Chromosome 20
Allele Paternal (confirmed)
Affects function (reported) Probably affects function
Affects function (concluded) Affects function
DNA change (genomic) (Relative to hg38 / GRCh38) g.3083006C>G
Published as -
Reference Davies et al. (2005)
DB-ID AVP_000008 See all 2 reported entries
Frequency -
Variant remarks -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     
AVP NM_000490.4 +?/+ 2 c.293G>C - r.(?) p.(Cys98Ser)