Fam174a Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

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

22 records found for search term Fam174a

Refine Term:

Assembly:

Chr

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
407508329	CV3435577	single nucleotide variant	NM_198507.3(FAM174A):c.7G>C (p.Ala3Pro)	not specified [RCV004625382]	uncertain significance	5	100535537	100535537	Human		name
405744025	CV3260033	single nucleotide variant	NM_198507.3(FAM174A):c.26G>C (p.Cys9Ser)	not specified [RCV004380988]	uncertain significance	5	100535556	100535556	Human		name
597738305	CV3668729	single nucleotide variant	NM_198507.3(FAM174A):c.24C>G (p.Cys8Trp)	not specified [RCV004921010]	uncertain significance	5	100535554	100535554	Human		name
156235065	CV2271307	single nucleotide variant	NM_198507.3(FAM174A):c.37C>G (p.Leu13Val)	not specified [RCV004136428]	uncertain significance	5	100535567	100535567	Human		name
329356789	CV2431146	single nucleotide variant	NM_198507.3(FAM174A):c.71C>T (p.Pro24Leu)	not specified [RCV004250498]	uncertain significance	5	100535601	100535601	Human		name
597738318	CV3668731	single nucleotide variant	NM_198507.3(FAM174A):c.76C>A (p.Leu26Ile)	not specified [RCV004921012]	uncertain significance	5	100535606	100535606	Human		name
156387102	CV2221402	single nucleotide variant	NM_198507.3(FAM174A):c.236C>A (p.Ser79Tyr)	not specified [RCV004096699]	uncertain significance	5	100535766	100535766	Human		name
156271144	CV2286312	single nucleotide variant	NM_198507.3(FAM174A):c.288C>A (p.His96Gln)	not specified [RCV004146263]	uncertain significance	5	100535818	100535818	Human		name
401886945	CV2777035	single nucleotide variant	NM_198507.3(FAM174A):c.160C>T (p.Pro54Ser)	not specified [RCV004351831]	uncertain significance	5	100535690	100535690	Human		name
401897024	CV2785510	single nucleotide variant	NM_198507.3(FAM174A):c.245G>A (p.Gly82Asp)	not specified [RCV004363035]	uncertain significance	5	100535775	100535775	Human		name
405743849	CV3260031	single nucleotide variant	NM_198507.3(FAM174A):c.203G>A (p.Arg68His)	not specified [RCV004380986]	uncertain significance	5	100535733	100535733	Human		name
405744018	CV3260032	single nucleotide variant	NM_198507.3(FAM174A):c.211G>C (p.Ala71Pro)	not specified [RCV004380987]	uncertain significance	5	100535741	100535741	Human		name
597738294	CV3668727	single nucleotide variant	NM_198507.3(FAM174A):c.110C>G (p.Ala37Gly)	not specified [RCV004921008]	uncertain significance	5	100535640	100535640	Human		name
156183953	CV2292197	single nucleotide variant	NM_198507.3(FAM174A):c.452G>A (p.Arg151Gln)	not specified [RCV004148246]	uncertain significance	5	100562071	100562071	Human		name
155913434	CV2341778	single nucleotide variant	NM_198507.3(FAM174A):c.365A>G (p.Gln122Arg)	not specified [RCV004184736]	uncertain significance	5	100535895	100535895	Human		name
401739947	CV2709744	single nucleotide variant	NM_198507.3(FAM174A):c.398G>T (p.Gly133Val)	not specified [RCV004320734]	uncertain significance	5	100535928	100535928	Human		name
405744033	CV3260034	single nucleotide variant	NM_198507.3(FAM174A):c.344C>G (p.Pro115Arg)	not specified [RCV004380989]	uncertain significance	5	100535874	100535874	Human		name
405744040	CV3260035	single nucleotide variant	NM_198507.3(FAM174A):c.437T>C (p.Met146Thr)	not specified [RCV004380990]	uncertain significance	5	100562056	100562056	Human		name
405744046	CV3260036	single nucleotide variant	NM_198507.3(FAM174A):c.440G>A (p.Arg147Lys)	not specified [RCV004380991]	uncertain significance	5	100562059	100562059	Human		name
405744051	CV3260037	single nucleotide variant	NM_198507.3(FAM174A):c.530A>T (p.Asp177Val)	not specified [RCV004380992]	uncertain significance	5	100562149	100562149	Human		name
597738287	CV3668726	single nucleotide variant	NM_198507.3(FAM174A):c.557A>T (p.Asn186Ile)	not specified [RCV004921007]	uncertain significance	5	100562176	100562176	Human		name
597738312	CV3668730	single nucleotide variant	NM_198507.3(FAM174A):c.304G>A (p.Glu102Lys)	not specified [RCV004921011]	uncertain significance	5	100535834	100535834	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