SNP Report
| Name | rs4938013 dbSNP Ensembl | ||
|---|---|---|---|
| Location | 11:113393748 - 113393748(+) | ||
| Variant Seq | C,T | ||
| Ancestral Allele | C | ||
| Ref Seq | A | ||
| Minor Allele Frequence | 0.339457 | ||
| Annotation | synonymous_variant; NMD_transcript_variant | ||
| Variant Effect | synonymous_variant(ENST00000303941, ENST00000542948); NMD_transcript_variant(ENST00000542948) | ||
| SIFT Annotation | deleterious; tolerated | ||
| SIFT Variant Effect | deleterious(ENST00000303941); tolerated(ENST00000542948) | ||
| PolyPhen Annotation | probably_damaging | ||
| PolyPhen Variant Effect | probably_damaging(ENST00000542948, ENST00000303941) | ||
| rSNP? | Yes Link in rVarBase | ||
| Related Regulatory Elements | n/a | ||
| Chromatin State | Weak transcription;Strong transcription | ||
| No. of Marker's Association Results | 0 (Positive: 0; Negative: 0; Trend: 0) | ||
| Source | LD-proxy | ||


