Product Details

SNP ID

rs73645468

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:35562896 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCACTTGTTCCACCACCTCCAGTGT[C/T]GGCTCCTCCAGCTGCCCCTCCGGCT

Phenotype

MIM: 611053

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FAM166B PubMed Links

Gene Details

Gene

FAM166B

Gene Name

family with sequence similarity 166 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001099951.3	542	Silent Mutation	CCA,CCG	P157P	NP_001093421.1
NM_001164310.2	542	Silent Mutation	CCA,CCG	P157P	NP_001157782.1
NM_001287238.1	542	Silent Mutation	CCA,CCG	P157P	NP_001274167.1
NM_001287239.1	542	Silent Mutation	CCA,CCG	P157P	NP_001274168.1
XM_011518028.2	542	Silent Mutation	CCA,CCG	P152P	XP_011516330.1

Gene

RUSC2

Gene Name

RUN and SH3 domain containing 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001135999.1	542	Intron			NP_001129471.1
XM_006716896.2	542	Intron			XP_006716959.1

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