Product Details

SNP ID

rs139473906

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:70052486 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGTTGCTGCTCTCCATGCCCACAGC[C/T]AGCCACTCCCCAGTGGGGCAGTAGC

Phenotype

MIM: 600190

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

TLE3 PubMed Links

Gene Details

Gene

TLE3

Gene Name

transducin like enhancer of split 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001105192.2	3165	Silent Mutation	CTA,CTG	L671L	NP_001098662.1
NM_001282979.1	3165	Silent Mutation	CTA,CTG	L666L	NP_001269908.1
NM_001282980.1	3165	Silent Mutation	CTA,CTG	L669L	NP_001269909.1
NM_001282981.1	3165	Silent Mutation	CTA,CTG	L664L	NP_001269910.1
NM_001282982.1	3165	Silent Mutation	CTA,CTG	L601L	NP_001269911.1
NM_005078.3	3165	Silent Mutation	CTA,CTG	L674L	NP_005069.2
NM_020908.2	3165	Silent Mutation	CTA,CTG	L662L	NP_065959.1
XM_005254622.4	3165	Silent Mutation	CTA,CTG	L681L	XP_005254679.1
XM_005254623.3	3165	Silent Mutation	CTA,CTG	L676L	XP_005254680.1
XM_005254625.3	3165	Silent Mutation	CTA,CTG	L672L	XP_005254682.1
XM_005254628.3	3165	Silent Mutation	CTA,CTG	L667L	XP_005254685.1
XM_005254633.2	3165	Silent Mutation	CTA,CTG	L657L	XP_005254690.1
XM_006720665.3	3165	Silent Mutation	CTA,CTG	L665L	XP_006720728.1
XM_011521976.2	3165	Silent Mutation	CTA,CTG	L684L	XP_011520278.1
XM_011521977.2	3165	Silent Mutation	CTA,CTG	L683L	XP_011520279.1
XM_011521978.2	3165	Silent Mutation	CTA,CTG	L679L	XP_011520280.1
XM_011521979.2	3165	Silent Mutation	CTA,CTG	L612L	XP_011520281.1
XM_011521980.2	3165	Silent Mutation	CTA,CTG	L673L	XP_011520282.1
XM_011521981.1	3165	Silent Mutation	CTA,CTG	L684L	XP_011520283.1
XM_011521982.2	3165	Silent Mutation	CTA,CTG	L600L	XP_011520284.1
XM_011521983.2	3165	Silent Mutation	CTA,CTG	L595L	XP_011520285.1
XM_017022532.1	3165	Intron			XP_016878021.1

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