Product Details
- SNP ID
-
rs34703432
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.3:172754574 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TTAACATCCACTACTGGGAGGACTA[C/G]CTTGGCAGACTCTTCCATTTTTGAT
- Phenotype
-
MIM: 600586
- Polymorphism
- C/G, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
ECT2
PubMed Links
Gene Details
- Gene
- ECT2
- Gene Name
- epithelial cell transforming 2
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001258315.1 |
516 |
Missense Mutation |
ACC,AGC |
T15S |
NP_001245244.1 |
NM_001258316.1 |
516 |
Missense Mutation |
ACC,AGC |
T15S |
NP_001245245.1 |
NM_018098.5 |
516 |
Missense Mutation |
ACC,AGC |
T15S |
NP_060568.3 |
XM_005247176.1 |
516 |
Missense Mutation |
ACC,AGC |
T15S |
XP_005247233.1 |
XM_006713523.3 |
516 |
Missense Mutation |
ACC,AGC |
T15S |
XP_006713586.1 |
XM_006713524.3 |
516 |
Missense Mutation |
ACC,AGC |
T15S |
XP_006713587.1 |
XM_011512514.2 |
516 |
Missense Mutation |
ACC,AGC |
T15S |
XP_011510816.1 |
XM_011512515.2 |
516 |
Missense Mutation |
ACC,AGC |
T15S |
XP_011510817.1 |
XM_011512516.1 |
516 |
Missense Mutation |
ACC,AGC |
T15S |
XP_011510818.1 |
XM_017005830.1 |
516 |
Missense Mutation |
ACC,AGC |
T15S |
XP_016861319.1 |
XM_017005831.1 |
516 |
Missense Mutation |
ACC,AGC |
T15S |
XP_016861320.1 |
XM_017005832.1 |
516 |
Missense Mutation |
ACC,AGC |
T15S |
XP_016861321.1 |
XM_017005833.1 |
516 |
Missense Mutation |
ACC,AGC |
T15S |
XP_016861322.1 |
XM_017005834.1 |
516 |
Missense Mutation |
ACC,AGC |
T15S |
XP_016861323.1 |
XM_017005835.1 |
516 |
Missense Mutation |
ACC,AGC |
T15S |
XP_016861324.1 |
XM_017005836.1 |
516 |
Missense Mutation |
ACC,AGC |
T15S |
XP_016861325.1 |
XM_017005837.1 |
516 |
Missense Mutation |
ACC,AGC |
T15S |
XP_016861326.1 |
XM_017005838.1 |
516 |
Missense Mutation |
ACC,AGC |
T15S |
XP_016861327.1 |
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