Genomic variant #0001973602

Chromosome X
DNA change (genomic) (Relative to hg19 / GRCh37) g.71358930A>G
Reference Copied from the Exome Variant Server
DB-ID NHSL2_000097
Frequency 1/10435
Freq. EA 0/6633
Freq. AA 1/3802
Owner Ivo F.A.C. Fokkema




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
NHSL2 NM_001013627.2 ?/? c.1532A>G r.(?) p.(Asp511Gly)