Snph Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)

32 records found for search term Snph

Refine Term:

Assembly:

Chr

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405715088	CV3326233	single nucleotide variant	NM_001318234.2(SNPH):c.284C>T (p.Thr95Met)	not specified [RCV004462376]	uncertain significance	20	1297246	1297246	Human		name
598171267	CV3915448	single nucleotide variant	NM_001318234.2(SNPH):c.221G>A (p.Gly74Asp)	not specified [RCV005284805]	uncertain significance	20	1297183	1297183	Human		name
156147798	CV2212861	single nucleotide variant	NM_001318234.2(SNPH):c.610G>A (p.Asp204Asn)	not specified [RCV004091519]	uncertain significance	20	1305047	1305047	Human		name
156017959	CV2302686	single nucleotide variant	NM_001318234.2(SNPH):c.607A>C (p.Lys203Gln)	not specified [RCV004162626]	uncertain significance	20	1305044	1305044	Human		name
156353273	CV2327505	single nucleotide variant	NM_001318234.2(SNPH):c.880G>A (p.Asp294Asn)	not specified [RCV004176816]	uncertain significance	20	1305317	1305317	Human		name
155964097	CV2330407	single nucleotide variant	NM_001318234.2(SNPH):c.316A>T (p.Ser106Cys)	not specified [RCV004180981]	uncertain significance	20	1300587	1300587	Human		name
329376631	CV2428488	single nucleotide variant	NM_001318234.2(SNPH):c.426C>A (p.Asp142Glu)	not specified [RCV004253276]	uncertain significance	20	1300697	1300697	Human		name
329384862	CV2454455	single nucleotide variant	NM_001318234.2(SNPH):c.923T>C (p.Leu308Pro)	not specified [RCV004267958]	uncertain significance	20	1305360	1305360	Human		name
401898426	CV2787894	single nucleotide variant	NM_001318234.2(SNPH):c.844G>A (p.Glu282Lys)	not specified [RCV004358571]	uncertain significance	20	1305281	1305281	Human		name
405715095	CV3326234	single nucleotide variant	NM_001318234.2(SNPH):c.580G>C (p.Asp194His)	not specified [RCV004462377]	uncertain significance	20	1305017	1305017	Human		name
407503641	CV3474638	single nucleotide variant	NM_001318234.2(SNPH):c.308C>T (p.Thr103Met)	not specified [RCV004670326]	uncertain significance	20	1300579	1300579	Human		name
597744862	CV3607045	single nucleotide variant	NM_001318234.2(SNPH):c.892C>T (p.Arg298Trp)	not specified [RCV004865552]	uncertain significance	20	1305329	1305329	Human		name
597744867	CV3607047	single nucleotide variant	NM_001318234.2(SNPH):c.514C>T (p.Arg172Cys)	not specified [RCV004865553]	uncertain significance	20	1304951	1304951	Human		name
597744871	CV3607048	single nucleotide variant	NM_001318234.2(SNPH):c.834C>A (p.Ser278Arg)	not specified [RCV004865554]	uncertain significance	20	1305271	1305271	Human		name
598238407	CV3915446	single nucleotide variant	NM_001318234.2(SNPH):c.343A>G (p.Thr115Ala)	not specified [RCV005275826]	uncertain significance	20	1300614	1300614	Human		name
598171263	CV3915447	single nucleotide variant	NM_001318234.2(SNPH):c.422A>G (p.Gln141Arg)	not specified [RCV005284804]	uncertain significance	20	1300693	1300693	Human		name
156031644	CV2202761	single nucleotide variant	NM_001318234.2(SNPH):c.1591C>A (p.Pro531Thr)	not specified [RCV004083000]	uncertain significance	20	1306028	1306028	Human		name
156070520	CV2232447	single nucleotide variant	NM_001318234.2(SNPH):c.1057A>T (p.Met353Leu)	not specified [RCV004099066]	uncertain significance	20	1305494	1305494	Human		name
156170560	CV2247390	single nucleotide variant	NM_001318234.2(SNPH):c.1322C>T (p.Ser441Leu)	not specified [RCV004108726]	uncertain significance	20	1305759	1305759	Human		name
156010321	CV2291000	single nucleotide variant	NM_001318234.2(SNPH):c.1386G>C (p.Lys462Asn)	not specified [RCV004151549]	uncertain significance	20	1305823	1305823	Human		name
155942519	CV2301220	single nucleotide variant	NM_001318234.2(SNPH):c.1175G>A (p.Cys392Tyr)	not specified [RCV004160124]	uncertain significance	20	1305612	1305612	Human		name
156092231	CV2302493	single nucleotide variant	NM_001318234.2(SNPH):c.1448C>T (p.Thr483Met)	not specified [RCV004161218]	uncertain significance	20	1305885	1305885	Human		name
329356994	CV2431216	single nucleotide variant	NM_001318234.2(SNPH):c.1007C>A (p.Thr336Asn)	not specified [RCV004250558]	uncertain significance	20	1305444	1305444	Human		name
329377034	CV2435785	single nucleotide variant	NM_001318234.2(SNPH):c.1291C>T (p.Arg431Trp)	not specified [RCV004253411]	uncertain significance	20	1305728	1305728	Human		name
401889812	CV2755014	single nucleotide variant	NM_001318234.2(SNPH):c.1600G>A (p.Gly534Ser)	not specified [RCV004335171]	uncertain significance	20	1306037	1306037	Human		name
401878204	CV2774030	single nucleotide variant	NM_001318234.2(SNPH):c.1066C>T (p.Arg356Cys)	not specified [RCV004345639]	uncertain significance	20	1305503	1305503	Human		name
405715082	CV3326232	single nucleotide variant	NM_001318234.2(SNPH):c.1604G>A (p.Gly535Asp)	not specified [RCV004462375]	uncertain significance	20	1306041	1306041	Human		name
407525287	CV3474637	single nucleotide variant	NM_001318234.2(SNPH):c.1466G>A (p.Arg489His)	not specified [RCV004679108]	uncertain significance	20	1305903	1305903	Human		name
597740785	CV3607046	single nucleotide variant	NM_001318234.2(SNPH):c.1388G>A (p.Ser463Asn)	not specified [RCV004864727]	uncertain significance	20	1305825	1305825	Human		name
597740791	CV3607049	single nucleotide variant	NM_001318234.2(SNPH):c.1375A>G (p.Lys459Glu)	not specified [RCV004864728]	uncertain significance	20	1305812	1305812	Human		name
598171260	CV3915445	single nucleotide variant	NM_001318234.2(SNPH):c.1607C>T (p.Ser536Phe)	not specified [RCV005284803]	uncertain significance	20	1306044	1306044	Human		name
598171272	CV3915449	single nucleotide variant	NM_001318234.2(SNPH):c.1481A>G (p.Gln494Arg)	not specified [RCV005284806]	uncertain significance	20	1305918	1305918	Human		name

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Create Name:

Description:

Send us a Message