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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