Genomic variant #0000611679

Individual ID 00000001
Chromosome 12
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.939302A>G
Reference dbSNP
DB-ID WNK1_000036
dbSNP ID rs10774466
Frequency 0.72635
Average frequency (large NGS studies) 0.68553 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Position     

RNA change     

Protein     
WNK1 NM_018979.3 ./. - c.1287A>G - r.(=) p.(=)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA arrayCNV - 904756 Admin