Product Details
- SNP ID
-
rs201002215
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.13:32442975 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TCCCAAAGTAATTTTTAGTCCATGG[A/T]TTTTTGTTAACAGGTCACATTTCTC
- Phenotype
-
MIM: 615788
- Polymorphism
- A/T, Transversion Substitution
- Allele Nomenclature
-
- Literature Links
-
N4BP2L2
PubMed Links
Gene Details
- Gene
- N4BP2L2
- Gene Name
- NEDD4 binding protein 2 like 2
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001278432.1 |
2987 |
Missense Mutation |
AAC,ATC |
N506I |
NP_001265361.1 |
NM_001320836.1 |
2987 |
Missense Mutation |
AAC,ATC |
N950I |
NP_001307765.1 |
NM_014887.2 |
2987 |
Intron |
|
|
NP_055702.1 |
NM_033111.4 |
2987 |
Missense Mutation |
AAC,ATC |
N521I |
NP_149102.3 |
XM_011534869.2 |
2987 |
Missense Mutation |
AAC,ATC |
N506I |
XP_011533171.1 |
XM_011534870.2 |
2987 |
Missense Mutation |
AAC,ATC |
N434I |
XP_011533172.1 |
XM_011534871.2 |
2987 |
Missense Mutation |
AAC,ATC |
N434I |
XP_011533173.1 |
XM_011534872.2 |
2987 |
Missense Mutation |
AAC,ATC |
N404I |
XP_011533174.1 |
XM_011534874.2 |
2987 |
Intron |
|
|
XP_011533176.1 |
XM_017020324.1 |
2987 |
Missense Mutation |
AAC,ATC |
N950I |
XP_016875813.1 |
XM_017020325.1 |
2987 |
Missense Mutation |
AAC,ATC |
N950I |
XP_016875814.1 |
XM_017020326.1 |
2987 |
Missense Mutation |
AAC,ATC |
N950I |
XP_016875815.1 |
XM_017020327.1 |
2987 |
Missense Mutation |
AAC,ATC |
N950I |
XP_016875816.1 |
XM_017020328.1 |
2987 |
Missense Mutation |
AAC,ATC |
N950I |
XP_016875817.1 |
XM_017020329.1 |
2987 |
Missense Mutation |
AAC,ATC |
N950I |
XP_016875818.1 |
XM_017020330.1 |
2987 |
Missense Mutation |
AAC,ATC |
N950I |
XP_016875819.1 |
XM_017020331.1 |
2987 |
Missense Mutation |
AAC,ATC |
N537I |
XP_016875820.1 |
XM_017020332.1 |
2987 |
Missense Mutation |
AAC,ATC |
N537I |
XP_016875821.1 |
XM_017020333.1 |
2987 |
Missense Mutation |
AAC,ATC |
N537I |
XP_016875822.1 |
XM_017020334.1 |
2987 |
Missense Mutation |
AAC,ATC |
N537I |
XP_016875823.1 |
XM_017020335.1 |
2987 |
Missense Mutation |
AAC,ATC |
N506I |
XP_016875824.1 |
XM_017020336.1 |
2987 |
Missense Mutation |
AAC,ATC |
N434I |
XP_016875825.1 |
XM_017020337.1 |
2987 |
Missense Mutation |
AAC,ATC |
N434I |
XP_016875826.1 |
XM_017020338.1 |
2987 |
Missense Mutation |
AAC,ATC |
N434I |
XP_016875827.1 |
XM_017020339.1 |
2987 |
Missense Mutation |
AAC,ATC |
N404I |
XP_016875828.1 |
XM_017020340.1 |
2987 |
Missense Mutation |
AAC,ATC |
N404I |
XP_016875829.1 |
XM_017020341.1 |
2987 |
Missense Mutation |
AAC,ATC |
N404I |
XP_016875830.1 |
XM_017020342.1 |
2987 |
Intron |
|
|
XP_016875831.1 |
XM_017020343.1 |
2987 |
Missense Mutation |
AAC,ATC |
N352I |
XP_016875832.1 |
XM_017020344.1 |
2987 |
Missense Mutation |
AAC,ATC |
N352I |
XP_016875833.1 |
XM_017020345.1 |
2987 |
Missense Mutation |
AAC,ATC |
N352I |
XP_016875834.1 |
XM_017020346.1 |
2987 |
Missense Mutation |
AAC,ATC |
N352I |
XP_016875835.1 |
XM_017020347.1 |
2987 |
Intron |
|
|
XP_016875836.1 |
XM_017020348.1 |
2987 |
Intron |
|
|
XP_016875837.1 |
XM_017020349.1 |
2987 |
Intron |
|
|
XP_016875838.1 |
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