Product Details
- SNP ID
-
rs145904278
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.12:44520075 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GGACCCGGTGAAGCGAACCACATTC[A/G]TTTCGTCCAGGCAAGTCTTGGTGAT
- Phenotype
-
MIM: 602320
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
NELL2
PubMed Links
Gene Details
- Gene
- NELL2
- Gene Name
- neural EGFL like 2
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001145107.1 |
2605 |
Missense Mutation |
ACG,ATG |
T827M |
NP_001138579.1 |
NM_001145108.1 |
2605 |
Missense Mutation |
ACG,ATG |
T777M |
NP_001138580.1 |
NM_001145109.1 |
2605 |
Missense Mutation |
ACG,ATG |
T776M |
NP_001138581.1 |
NM_001145110.1 |
2605 |
Missense Mutation |
ACG,ATG |
T800M |
NP_001138582.1 |
NM_006159.2 |
2605 |
Missense Mutation |
ACG,ATG |
T777M |
NP_006150.1 |
XM_005268905.3 |
2605 |
Missense Mutation |
ACG,ATG |
T777M |
XP_005268962.1 |
XM_011538396.1 |
2605 |
Missense Mutation |
ACG,ATG |
T777M |
XP_011536698.1 |
XM_017019341.1 |
2605 |
Missense Mutation |
ACG,ATG |
T832M |
XP_016874830.1 |
XM_017019342.1 |
2605 |
Missense Mutation |
ACG,ATG |
T782M |
XP_016874831.1 |
XM_017019343.1 |
2605 |
Missense Mutation |
ACG,ATG |
T782M |
XP_016874832.1 |
XM_017019344.1 |
2605 |
Missense Mutation |
ACG,ATG |
T782M |
XP_016874833.1 |
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