Product Details

SNP ID

rs201572962

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:3225147 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTGGATTCAGGAGGCTTGGTTGCAC[A/G]CCAGTCTCGAGAACAGGCTGCATGC

Phenotype

MIM: 601337

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

RFX3 PubMed Links

Gene Details

Gene

RFX3

Gene Name

regulatory factor X3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001282116.1	2466	Silent Mutation	GGC,GGT	G715G	NP_001269045.1
NM_001282117.1	2466	Intron			NP_001269046.1
NM_002919.3	2466	Intron			NP_002910.1
NM_134428.2	2466	Silent Mutation	GGC,GGT	G715G	NP_602304.1
XM_006716840.1	2466	Silent Mutation	GGC,GGT	G746G	XP_006716903.1
XM_006716843.1	2466	Silent Mutation	GGC,GGT	G736G	XP_006716906.1
XM_006716844.1	2466	Silent Mutation	GGC,GGT	G736G	XP_006716907.1
XM_006716845.2	2466	Silent Mutation	GGC,GGT	G736G	XP_006716908.1
XM_006716847.3	2466	Silent Mutation	GGC,GGT	G458G	XP_006716910.1
XM_011517998.1	2466	Silent Mutation	GGC,GGT	G736G	XP_011516300.1
XM_011517999.1	2466	Silent Mutation	GGC,GGT	G736G	XP_011516301.1
XM_011518000.1	2466	Silent Mutation	GGC,GGT	G711G	XP_011516302.1
XM_011518001.1	2466	Silent Mutation	GGC,GGT	G653G	XP_011516303.1
XM_017015000.1	2466	Silent Mutation	GGC,GGT	G736G	XP_016870489.1
XM_017015001.1	2466	Silent Mutation	GGC,GGT	G690G	XP_016870490.1
XM_017015002.1	2466	Silent Mutation	GGC,GGT	G467G	XP_016870491.1

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