Product Details

SNP ID

rs139741665

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:18232526 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGCACCTGGCGTGGAGTTCACAGGC[C/T]TGCACCGGGATGCAGCCACTGTCAC

Phenotype

MIM: 600966

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

LLGL1 PubMed Links

Gene Details

Gene

LLGL1

Gene Name

LLGL1, scribble cell polarity complex component

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004140.3	272	Silent Mutation	CTG,TTG	L71L	NP_004131.3
XM_011523849.2	272	Silent Mutation	CTG,TTG	L71L	XP_011522151.1
XM_011523850.2	272	Silent Mutation	CTG,TTG	L71L	XP_011522152.1
XM_011523851.2	272	Silent Mutation	CTG,TTG	L71L	XP_011522153.1
XM_011523852.2	272	Silent Mutation	CTG,TTG	L71L	XP_011522154.1
XM_011523853.2	272	Silent Mutation	CTG,TTG	L71L	XP_011522155.1
XM_011523854.2	272	Silent Mutation	CTG,TTG	L71L	XP_011522156.1
XM_011523855.2	272	Silent Mutation	CTG,TTG	L71L	XP_011522157.1
XM_011523856.1	272	Silent Mutation	CTG,TTG	L71L	XP_011522158.1

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