Genomic variant #0000000768

Individual ID 00000003
Chromosome 1
Allele Parent #2
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.75149341A>G
Reference dbSNP
DB-ID LHX8_000004 See all 10 reported entries
Frequency 0.500 Patients_Q37.0
Allele Count 1
Allele Number 2
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.810+659A>G - r.(=) p.(=) -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000004 DNA TaqMan - 145 Admin