Product Details

SNP ID

rs3748932

Assay Type

DME

NCBI dbSNP Submissions

NA

Location

Chr.2:100393544 on Build GRCh38

Set Membership

HapMap DME Validated Inventoried

Context Sequence [VIC/FAM]

TACGTCACCCAGTGAATGATGTGGT[C/T]CCCAAACTGAAGGTCTAGCCATCTG

Phenotype

MIM: 606376

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

CHST10 PubMed Links

Gene Details

Gene

CHST10

Gene Name

carbohydrate sulfotransferase 10

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004854.4	1494	Missense Mutation			NP_004845.1
XM_011512207.1	1494	Missense Mutation			XP_011510509.1
XM_011512208.1	1494	Missense Mutation			XP_011510510.1
XM_011512210.1	1494	Missense Mutation			XP_011510512.1
XM_011512211.1	1494	Missense Mutation			XP_011510513.1
XM_011512212.1	1494	Missense Mutation			XP_011510514.1
XM_017005380.1	1494	Missense Mutation			XP_016860869.1
XM_017005381.1	1494	Missense Mutation			XP_016860870.1
XM_017005382.1	1494	Missense Mutation			XP_016860871.1
XM_017005383.1	1494	Missense Mutation			XP_016860872.1

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