Genomic variant #0000124763

Individual ID 00000001
Chromosome 2
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.204259854T>G
Reference -
DB-ID ABI2_000035
dbSNP ID rs1324090399
Frequency 0.001938
Allele Count 1
Allele Number 516
Combined Depth 4101
Homozygous 0
Heterozygote 1
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)     

RNA change     

Protein     
ABI2 NM_005759.4 ./. - c.707+285T>G r.(=) p.(=)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin