Product Details
- SNP ID
-
rs200691018
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
5
- Location
-
Chr.1:155014961 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CTTTGTAGGGCCAGAGGCACTAGGC[A/G]CCCTCCTTGAATTTGCCTATACAGC
- Phenotype
-
MIM: 607646
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
DCST2
PubMed Links
Gene Details
- Gene
- DCST2
- Gene Name
- DC-STAMP domain containing 2
There are no transcripts associated with this gene.
- Gene
- ZBTB7B
- Gene Name
- zinc finger and BTB domain containing 7B
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001252406.2 |
628 |
Missense Mutation |
ACC,GCC |
T135A |
NP_001239335.1 |
NM_001256455.1 |
628 |
Missense Mutation |
ACC,GCC |
T101A |
NP_001243384.1 |
XM_006711349.2 |
628 |
Missense Mutation |
ACC,GCC |
T101A |
XP_006711412.2 |
XM_006711353.1 |
628 |
Missense Mutation |
ACC,GCC |
T101A |
XP_006711416.1 |
XM_006711354.1 |
628 |
Missense Mutation |
ACC,GCC |
T101A |
XP_006711417.1 |
XM_006711356.3 |
628 |
Missense Mutation |
ACC,GCC |
T101A |
XP_006711419.1 |
XM_006711357.1 |
628 |
Missense Mutation |
ACC,GCC |
T101A |
XP_006711420.1 |
XM_006711358.1 |
628 |
Missense Mutation |
ACC,GCC |
T101A |
XP_006711421.1 |
XM_006711359.2 |
628 |
Missense Mutation |
ACC,GCC |
T101A |
XP_006711422.1 |
XM_011509598.2 |
628 |
Missense Mutation |
ACC,GCC |
T135A |
XP_011507900.1 |
XM_011509599.2 |
628 |
Missense Mutation |
ACC,GCC |
T101A |
XP_011507901.1 |
XM_017001399.1 |
628 |
Missense Mutation |
ACC,GCC |
T192A |
XP_016856888.1 |
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