Product Details

SNP ID

rs199946051

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.20:62126416 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCGGCCAGCTCCCTGCTCAGCCAGC[A/G]GTATGCCGCCTCCCTGGGTCTAGGT

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

LSM14B PubMed Links

Gene Details

Gene

LSM14B

Gene Name

LSM family member 14B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_144703.2	607	Missense Mutation	CAG,CGG	Q135R	NP_653304.2
XM_005260302.3	607	Missense Mutation	CAG,CGG	Q135R	XP_005260359.1
XM_011528605.2	607	Missense Mutation	CAG,CGG	Q161R	XP_011526907.1
XM_011528606.2	607	Missense Mutation	CAG,CGG	Q135R	XP_011526908.1
XM_011528607.2	607	Missense Mutation	CAG,CGG	Q161R	XP_011526909.1
XM_011528608.2	607	Missense Mutation	CAG,CGG	Q161R	XP_011526910.1
XM_011528609.2	607	Missense Mutation	CAG,CGG	Q161R	XP_011526911.1
XM_011528611.2	607	Missense Mutation	CAG,CGG	Q135R	XP_011526913.1
XM_011528612.2	607	Missense Mutation	CAG,CGG	Q16R	XP_011526914.1
XM_011528613.2	607	Missense Mutation	CAG,CGG	Q16R	XP_011526915.1
XM_011528614.2	607	Missense Mutation	CAG,CGG	Q16R	XP_011526916.1
XM_011528615.2	607	Intron			XP_011526917.1
XM_017027688.1	607	Missense Mutation	CAG,CGG	Q161R	XP_016883177.1
XM_017027689.1	607	Missense Mutation	CAG,CGG	Q135R	XP_016883178.1
XM_017027690.1	607	Intron			XP_016883179.1

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