SNP Report
Name | rs80087508 dbSNP Ensembl | ||
---|---|---|---|
Location | 15:78589891 - 78589891(+) | ||
Variant Seq | G | ||
Ancestral Allele | A | ||
Ref Seq | A | ||
Minor Allele Frequence | 0.00419329 | ||
Annotation | downstream_gene_variant; non_coding_transcript_exon_variant; missense_variant; upstream_gene_variant; intron_variant; non_coding_transcript_variant | ||
Variant Effect | downstream_gene_variant(ENST00000348639, ENST00000559658, ENST00000559002); non_coding_transcript_exon_variant(ENST00000567141); missense_variant(ENST00000394802, ENST00000299565); upstream_gene_variant(ENST00000559576); intron_variant(ENST00000559554); non_coding_transcript_variant(ENST00000567141) | ||
SIFT Annotation | deleterious | ||
SIFT Variant Effect | deleterious(ENST00000394802, ENST00000299565) | ||
PolyPhen Annotation | probably_damaging | ||
PolyPhen Variant Effect | probably_damaging(ENST00000394802, ENST00000299565) | ||
rSNP? | Yes Link in rVarBase | ||
Related Regulatory Elements | n/a | ||
Chromatin State | Weak transcription;Strong transcription | ||
No. of Marker's Association Results | 1 (Positive: 1; Negative: 0; Trend: 0) | ||
Source | Literature |