Product Details
- SNP ID
-
rs2297775
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
65
- Location
-
Chr.1:155765221 on Build GRCh38
- Set Membership
-
HapMap
JSNP
- Context Sequence [VIC/FAM]
- CTACTAAGCCTCACTTCAGGATCCA[C/T]TGAGGACAAAGCATTCTTTGATGAT
- Phenotype
-
MIM: 610393
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
GON4L
PubMed Links
Gene Details
- Gene
- GON4L
- Gene Name
- gon-4 like
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001282856.1 |
4391 |
Missense Mutation |
ATG,GTG |
M1418V |
NP_001269785.1 |
NM_001282858.1 |
4391 |
Missense Mutation |
ATG,GTG |
M1418V |
NP_001269787.1 |
NM_001282860.1 |
4391 |
Missense Mutation |
ATG,GTG |
M1418V |
NP_001269789.1 |
NM_001282861.1 |
4391 |
Missense Mutation |
ATG,GTG |
M1418V |
NP_001269790.1 |
NM_032292.5 |
4391 |
Missense Mutation |
ATG,GTG |
M1418V |
NP_115668.4 |
XM_005245284.3 |
4391 |
Missense Mutation |
ATG,GTG |
M1246V |
XP_005245341.1 |
XM_005245286.3 |
4391 |
Missense Mutation |
ATG,GTG |
M614V |
XP_005245343.1 |
XM_006711393.3 |
4391 |
Missense Mutation |
ATG,GTG |
M1418V |
XP_006711456.1 |
XM_006711394.3 |
4391 |
Missense Mutation |
ATG,GTG |
M1418V |
XP_006711457.1 |
XM_011509658.2 |
4391 |
Missense Mutation |
ATG,GTG |
M1389V |
XP_011507960.1 |
XM_011509659.2 |
4391 |
Missense Mutation |
ATG,GTG |
M1246V |
XP_011507961.1 |
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