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 |