Product Details

SNP ID

rs201842409

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.20:62126392 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGGATGGCGCCCTACGGCCCGCTGG[C/T]GGCCAGCTCCCTGCTCAGCCAGCAG

Phenotype

Polymorphism

C/T, 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	583	Missense Mutation	GCG,GTG	A127V	NP_653304.2
XM_005260302.3	583	Missense Mutation	GCG,GTG	A127V	XP_005260359.1
XM_011528605.2	583	Missense Mutation	GCG,GTG	A153V	XP_011526907.1
XM_011528606.2	583	Missense Mutation	GCG,GTG	A127V	XP_011526908.1
XM_011528607.2	583	Missense Mutation	GCG,GTG	A153V	XP_011526909.1
XM_011528608.2	583	Missense Mutation	GCG,GTG	A153V	XP_011526910.1
XM_011528609.2	583	Missense Mutation	GCG,GTG	A153V	XP_011526911.1
XM_011528611.2	583	Missense Mutation	GCG,GTG	A127V	XP_011526913.1
XM_011528612.2	583	Missense Mutation	GCG,GTG	A8V	XP_011526914.1
XM_011528613.2	583	Missense Mutation	GCG,GTG	A8V	XP_011526915.1
XM_011528614.2	583	Missense Mutation	GCG,GTG	A8V	XP_011526916.1
XM_011528615.2	583	Intron			XP_011526917.1
XM_017027688.1	583	Missense Mutation	GCG,GTG	A153V	XP_016883177.1
XM_017027689.1	583	Missense Mutation	GCG,GTG	A127V	XP_016883178.1
XM_017027690.1	583	Intron			XP_016883179.1

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