Product Details

SNP ID

rs113926971

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:132490786 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGCGTCCCCCGCGCCGCCGCCGCCG[A/C]GAGTCCAGCTCGCAGGAGGAGGAGG

Phenotype

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

FBRSL1 PubMed Links

Gene Details

Gene

FBRSL1

Gene Name

fibrosin like 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001142641.1	322	Silent Mutation	CGA,CGC	R72R	NP_001136113.1
XM_005266171.3	322	Silent Mutation	CGA,CGC	R72R	XP_005266228.1
XM_005266173.3	322	Silent Mutation	CGA,CGC	R72R	XP_005266230.1
XM_005266175.3	322	Silent Mutation	CGA,CGC	R72R	XP_005266232.1
XM_005266176.3	322	Silent Mutation	CGA,CGC	R72R	XP_005266233.1
XM_005266177.3	322	Silent Mutation	CGA,CGC	R72R	XP_005266234.1
XM_005266181.3	322	Silent Mutation	CGA,CGC	R72R	XP_005266238.1
XM_011534803.2	322	Silent Mutation	CGA,CGC	R72R	XP_011533105.1
XM_011534804.2	322	Silent Mutation	CGA,CGC	R72R	XP_011533106.1
XM_011534805.2	322	Silent Mutation	CGA,CGC	R72R	XP_011533107.1
XM_011534806.2	322	Silent Mutation	CGA,CGC	R72R	XP_011533108.1
XM_011534807.2	322	Silent Mutation	CGA,CGC	R72R	XP_011533109.1
XM_011534808.2	322	Silent Mutation	CGA,CGC	R72R	XP_011533110.1
XM_011534809.2	322	Silent Mutation	CGA,CGC	R72R	XP_011533111.1
XM_011534810.2	322	Silent Mutation	CGA,CGC	R72R	XP_011533112.1
XM_011534812.2	322	UTR 5			XP_011533114.1
XM_011534816.2	322	Silent Mutation	CGA,CGC	R72R	XP_011533118.1

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