Product Details

SNP ID

rs147539143

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:139060468 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TATAGGGGATGAATTTTTTCCACTG[C/T]GAACAGAGGATGCTGCTTTCAGGAG

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

ELF2 PubMed Links

Gene Details

Gene

ELF2

Gene Name

E74 like ETS transcription factor 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001276457.1	1057	Missense Mutation	CAC,CGC	H249R	NP_001263386.1
NM_001276458.1	1057	Missense Mutation	CAC,CGC	H266R	NP_001263387.1
NM_001276459.1	1057	Missense Mutation	CAC,CGC	H237R	NP_001263388.1
NM_006874.3	1057	Missense Mutation	CAC,CGC	H278R	NP_006865.1
NM_201999.2	1057	Missense Mutation	CAC,CGC	H326R	NP_973728.1
XM_005262803.2	1057	Missense Mutation	CAC,CGC	H338R	XP_005262860.1
XM_005262804.2	1057	Missense Mutation	CAC,CGC	H326R	XP_005262861.1
XM_005262805.2	1057	Missense Mutation	CAC,CGC	H297R	XP_005262862.1
XM_006714128.2	1057	Missense Mutation	CAC,CGC	H309R	XP_006714191.1
XM_006714129.3	1057	Missense Mutation	CAC,CGC	H234R	XP_006714192.1
XM_011531710.2	1057	Missense Mutation	CAC,CGC	H234R	XP_011530012.1
XM_011531711.2	1057	Missense Mutation	CAC,CGC	H234R	XP_011530013.1
XM_011531712.2	1057	Missense Mutation	CAC,CGC	H234R	XP_011530014.1
XM_011531714.2	1057	Missense Mutation	CAC,CGC	H80R	XP_011530016.1
XM_017007856.1	1057	Missense Mutation	CAC,CGC	H222R	XP_016863345.1
XM_017007857.1	1057	Missense Mutation	CAC,CGC	H222R	XP_016863346.1
XM_017007858.1	1057	Missense Mutation	CAC,CGC	H205R	XP_016863347.1
XM_017007859.1	1057	Missense Mutation	CAC,CGC	H193R	XP_016863348.1
XM_017007860.1	1057	Missense Mutation	CAC,CGC	H193R	XP_016863349.1
XM_017007861.1	1057	Missense Mutation	CAC,CGC	H193R	XP_016863350.1

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