Product Details

SNP ID

rs143836571

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:100393303 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAAGAGCTTAAAGTCCCCTTCGAAA[C/T]GGGCATACAGGCGTCGGATGTCTCG

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	1735	Missense Mutation	CAT,CGT	H338R	NP_004845.1
XM_011512207.1	1735	Missense Mutation	CAT,CGT	H338R	XP_011510509.1
XM_011512208.1	1735	Missense Mutation	CAT,CGT	H338R	XP_011510510.1
XM_011512210.1	1735	Missense Mutation	CAT,CGT	H338R	XP_011510512.1
XM_011512211.1	1735	Missense Mutation	CAT,CGT	H338R	XP_011510513.1
XM_011512212.1	1735	Missense Mutation	CAT,CGT	H338R	XP_011510514.1
XM_017005380.1	1735	Missense Mutation	CAT,CGT	H338R	XP_016860869.1
XM_017005381.1	1735	Missense Mutation	CAT,CGT	H338R	XP_016860870.1
XM_017005382.1	1735	Missense Mutation	CAT,CGT	H338R	XP_016860871.1
XM_017005383.1	1735	Missense Mutation	CAT,CGT	H338R	XP_016860872.1

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