Product Details

SNP ID

rs11854484

Assay Type

DME

NCBI dbSNP Submissions

NA

Location

Chr.15:45253280 on Build GRCh38

Set Membership

DME Validated Inventoried

Context Sequence [VIC/FAM]

ACAGTGGAGACTGGCACAGTGAACC[C/T]GGGGCTGGAGCTCATGGTAATCACC

Phenotype

MIM: 606208

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

LOC101928414 PubMed Links

Gene Details

Gene

LOC101928414

Gene Name

uncharacterized LOC101928414

There are no transcripts associated with this gene.

Gene

SLC28A2

Gene Name

solute carrier family 28 member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004212.3	101	Missense Mutation	CCG,CTG	P22L	NP_004203.2
XM_011522198.2	101	Missense Mutation	CCG,CTG	P22L	XP_011520500.1
XM_011522199.1	101	Missense Mutation	CCG,CTG	P22L	XP_011520501.1
XM_011522200.2	101	Missense Mutation	CCG,CTG	P22L	XP_011520502.1
XM_011522201.2	101	Missense Mutation	CCG,CTG	P22L	XP_011520503.1
XM_011522202.2	101	Intron			XP_011520504.1

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