Product Details
- SNP ID
-
rs10936352
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.3:100754661 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TGTTGCTGACCGGGCCTTCACCAAG[C/T]GGGTTTTTGGGTTTCACCTGGAATT
- Phenotype
-
MIM: 606279
MIM: 602498
- Polymorphism
- C/T, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
ABI3BP
PubMed Links
Gene Details
- Gene
- ABI3BP
- Gene Name
- ABI family member 3 binding protein
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_015429.3 |
4855 |
Silent Mutation |
CCA,CCG |
P916P |
NP_056244.2 |
XM_005247281.2 |
4855 |
Silent Mutation |
CCA,CCG |
P1634P |
XP_005247338.1 |
XM_005247282.2 |
4855 |
Silent Mutation |
CCA,CCG |
P1620P |
XP_005247339.1 |
XM_005247283.2 |
4855 |
Silent Mutation |
CCA,CCG |
P1618P |
XP_005247340.1 |
XM_005247284.2 |
4855 |
Silent Mutation |
CCA,CCG |
P1615P |
XP_005247341.1 |
XM_005247285.2 |
4855 |
Silent Mutation |
CCA,CCG |
P1614P |
XP_005247342.1 |
XM_005247287.2 |
4855 |
Silent Mutation |
CCA,CCG |
P1612P |
XP_005247344.1 |
XM_005247288.2 |
4855 |
Silent Mutation |
CCA,CCG |
P1610P |
XP_005247345.1 |
XM_005247289.2 |
4855 |
Silent Mutation |
CCA,CCG |
P1609P |
XP_005247346.1 |
XM_005247290.2 |
4855 |
Silent Mutation |
CCA,CCG |
P1609P |
XP_005247347.1 |
XM_005247291.2 |
4855 |
Silent Mutation |
CCA,CCG |
P1608P |
XP_005247348.1 |
XM_005247293.2 |
4855 |
Silent Mutation |
CCA,CCG |
P1598P |
XP_005247350.1 |
XM_005247294.2 |
4855 |
Silent Mutation |
CCA,CCG |
P1595P |
XP_005247351.1 |
XM_005247295.2 |
4855 |
Silent Mutation |
CCA,CCG |
P1588P |
XP_005247352.1 |
XM_005247296.2 |
4855 |
Silent Mutation |
CCA,CCG |
P1587P |
XP_005247353.1 |
XM_005247298.2 |
4855 |
Silent Mutation |
CCA,CCG |
P1586P |
XP_005247355.1 |
XM_005247299.3 |
4855 |
Silent Mutation |
CCA,CCG |
P1585P |
XP_005247356.1 |
XM_005247300.2 |
4855 |
Silent Mutation |
CCA,CCG |
P1576P |
XP_005247357.1 |
XM_005247301.2 |
4855 |
Silent Mutation |
CCA,CCG |
P1567P |
XP_005247358.1 |
XM_005247302.2 |
4855 |
Silent Mutation |
CCA,CCG |
P1566P |
XP_005247359.1 |
XM_005247303.2 |
4855 |
Silent Mutation |
CCA,CCG |
P1547P |
XP_005247360.1 |
XM_005247305.2 |
4855 |
Silent Mutation |
CCA,CCG |
P1519P |
XP_005247362.1 |
XM_005247306.2 |
4855 |
Silent Mutation |
CCA,CCG |
P1498P |
XP_005247363.1 |
XM_005247309.1 |
4855 |
Silent Mutation |
CCA,CCG |
P1336P |
XP_005247366.1 |
XM_006713569.2 |
4855 |
Silent Mutation |
CCA,CCG |
P1583P |
XP_006713632.1 |
XM_006713570.2 |
4855 |
Silent Mutation |
CCA,CCG |
P1572P |
XP_006713633.1 |
XM_006713571.2 |
4855 |
Silent Mutation |
CCA,CCG |
P1562P |
XP_006713634.1 |
XM_006713572.2 |
4855 |
Silent Mutation |
CCA,CCG |
P1560P |
XP_006713635.1 |
XM_011512639.1 |
4855 |
Silent Mutation |
CCA,CCG |
P1614P |
XP_011510941.1 |
XM_011512640.1 |
4855 |
Silent Mutation |
CCA,CCG |
P1612P |
XP_011510942.1 |
XM_011512641.1 |
4855 |
Silent Mutation |
CCA,CCG |
P1609P |
XP_011510943.1 |
XM_011512643.1 |
4855 |
Silent Mutation |
CCA,CCG |
P1607P |
XP_011510945.1 |
XM_011512644.1 |
4855 |
Silent Mutation |
CCA,CCG |
P1606P |
XP_011510946.1 |
XM_011512645.1 |
4855 |
Silent Mutation |
CCA,CCG |
P1606P |
XP_011510947.1 |
XM_011512646.1 |
4855 |
Silent Mutation |
CCA,CCG |
P1603P |
XP_011510948.1 |
XM_011512647.1 |
4855 |
Silent Mutation |
CCA,CCG |
P1589P |
XP_011510949.1 |
XM_011512648.1 |
4855 |
Silent Mutation |
CCA,CCG |
P1588P |
XP_011510950.1 |
XM_011512649.1 |
4855 |
Silent Mutation |
CCA,CCG |
P1586P |
XP_011510951.1 |
XM_011512651.1 |
4855 |
Silent Mutation |
CCA,CCG |
P1567P |
XP_011510953.1 |
XM_011512652.1 |
4855 |
Silent Mutation |
CCA,CCG |
P1563P |
XP_011510954.1 |
XM_011512653.1 |
4855 |
Silent Mutation |
CCA,CCG |
P1560P |
XP_011510955.1 |
XM_011512654.1 |
4855 |
Silent Mutation |
CCA,CCG |
P1557P |
XP_011510956.1 |
XM_011512656.1 |
4855 |
Silent Mutation |
CCA,CCG |
P1535P |
XP_011510958.1 |
XM_011512657.1 |
4855 |
Silent Mutation |
CCA,CCG |
P1534P |
XP_011510959.1 |
XM_011512658.1 |
4855 |
Silent Mutation |
CCA,CCG |
P1530P |
XP_011510960.1 |
XM_011512659.1 |
4855 |
Silent Mutation |
CCA,CCG |
P1523P |
XP_011510961.1 |
XM_011512660.1 |
4855 |
Silent Mutation |
CCA,CCG |
P1513P |
XP_011510962.1 |
XM_017006105.1 |
4855 |
Silent Mutation |
CCA,CCG |
P1615P |
XP_016861594.1 |
XM_017006106.1 |
4855 |
Silent Mutation |
CCA,CCG |
P1609P |
XP_016861595.1 |
XM_017006107.1 |
4855 |
Silent Mutation |
CCA,CCG |
P1565P |
XP_016861596.1 |
XM_017006108.1 |
4855 |
Silent Mutation |
CCA,CCG |
P1535P |
XP_016861597.1 |
- Gene
- TFG
- Gene Name
- TRK-fused gene
There are no transcripts associated with this gene.
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