Product Details

SNP ID

rs143174853

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:66366157 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCCCAGGACTGGTGGAGCTGGTCAC[C/T]ATGGCTGTGATGGCGGGGAAGACGG

Phenotype

MIM: 602110

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

LOC102724064 PubMed Links

Gene Details

Gene

LOC102724064

Gene Name

uncharacterized LOC102724064

There are no transcripts associated with this gene.

Gene

SLC29A2

Gene Name

solute carrier family 29 member 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001300868.1	1322	Missense Mutation	ATA,ATG	I314M	NP_001287797.1
NM_001300869.1	1322	Missense Mutation	AGT,GGT	S270G	NP_001287798.1
NM_001532.2	1322	Missense Mutation	ATA,ATG	I314M	NP_001523.2
XM_011544974.1	1322	Missense Mutation	AGT,GGT	S381G	XP_011543276.1
XM_017017630.1	1322	Missense Mutation	AGT,GGT	S381G	XP_016873119.1
XM_017017631.1	1322	Missense Mutation	ATA,ATG	I314M	XP_016873120.1
XM_017017632.1	1322	Missense Mutation	ATA,ATG	I314M	XP_016873121.1
XM_017017633.1	1322	Missense Mutation	AGT,GGT	S381G	XP_016873122.1
XM_017017634.1	1322	Missense Mutation	ATA,ATG	I256M	XP_016873123.1
XM_017017635.1	1322	Missense Mutation	ATA,ATG	I256M	XP_016873124.1
XM_017017636.1	1322	Missense Mutation	ATA,ATG	I314M	XP_016873125.1
XM_017017637.1	1322	Missense Mutation	AGT,GGT	S270G	XP_016873126.1
XM_017017638.1	1322	Missense Mutation	AGT,GGT	S261G	XP_016873127.1

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