Genomic variant #0001973528

Chromosome X
DNA change (genomic) (Relative to hg19 / GRCh37) g.71344303T>C
Reference Copied from the Exome Variant Server
DB-ID NHSL2_000028
Frequency 2175/3600
Freq. EA 1914/2391
Freq. AA 261/1209
Owner Ivo F.A.C. Fokkema




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
NHSL2 NM_001013627.2 ?/? c.281-7626T>C r.(=) p.(=)