Genomic variant #0000001087

Individual ID 00000005
Chromosome 1
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.75143364A>C
Reference dbSNP
DB-ID LHX8_000006 See all 7 reported entries
Frequency 0.500 Patients_Q37.3_left
Allele Count 2
Allele Number 4
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     
LHX8 NM_001001933.1 ./. - c.610+26A>C - r.(=) p.(=) -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000006 DNA TaqMan - 171 Admin