Product Details

SNP ID

rs111524366

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:81585545 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCAGGGACAGCACGCAGCTCTCATG[C/T]AGGTGCAGCTGGTACTTGTCAGGCT

Phenotype

MIM: 600189

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

TLE1 PubMed Links

Gene Details

Gene

TLE1

Gene Name

transducin like enhancer of split 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001303103.1	2324	Silent Mutation	CTA,CTG	L706L	NP_001290032.1
NM_001303104.1	2324	Silent Mutation	CTA,CTG	L681L	NP_001290033.1
NM_005077.4	2324	Silent Mutation	CTA,CTG	L696L	NP_005068.2
XM_005252151.1	2324	Silent Mutation	CTA,CTG	L740L	XP_005252208.1
XM_005252152.1	2324	Silent Mutation	CTA,CTG	L739L	XP_005252209.1
XM_005252153.1	2324	Silent Mutation	CTA,CTG	L730L	XP_005252210.1
XM_005252154.1	2324	Silent Mutation	CTA,CTG	L729L	XP_005252211.1
XM_005252156.2	2324	Silent Mutation	CTA,CTG	L705L	XP_005252213.1
XM_005252162.1	2324	Silent Mutation	CTA,CTG	L656L	XP_005252219.1
XM_005252163.2	2324	Silent Mutation	CTA,CTG	L622L	XP_005252220.1
XM_006717258.1	2324	Silent Mutation	CTA,CTG	L739L	XP_006717321.1
XM_006717259.3	2324	Silent Mutation	CTA,CTG	L684L	XP_006717322.1
XM_006717260.1	2324	Silent Mutation	CTA,CTG	L666L	XP_006717323.1
XM_006717261.2	2324	Silent Mutation	CTA,CTG	L625L	XP_006717324.1
XM_006717262.1	2324	Silent Mutation	CTA,CTG	L695L	XP_006717325.1
XM_006717263.1	2324	Silent Mutation	CTA,CTG	L694L	XP_006717326.1
XM_011518951.2	2324	Silent Mutation	CTA,CTG	L695L	XP_011517253.1
XM_017015064.1	2324	Silent Mutation	CTA,CTG	L705L	XP_016870553.1
XM_017015065.1	2324	Silent Mutation	CTA,CTG	L704L	XP_016870554.1
XM_017015066.1	2324	Silent Mutation	CTA,CTG	L650L	XP_016870555.1

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