Product Details
- SNP ID
-
rs201091355
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.20:59865851 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GATATGCACTGAACTTCTGAAATAT[A/C]TTTTCCCAAAAGTCCTAAATTAATT
- Phenotype
-
MIM: 604105
- Polymorphism
- A/C, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
SYCP2
PubMed Links
Gene Details
- Gene
- SYCP2
- Gene Name
- synaptonemal complex protein 2
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_014258.3 |
4520 |
Missense Mutation |
AAG,AAT |
K1445N |
NP_055073.2 |
XM_011528487.2 |
4520 |
Missense Mutation |
AAG,AAT |
K1452N |
XP_011526789.1 |
XM_011528488.2 |
4520 |
Missense Mutation |
AAG,AAT |
K1452N |
XP_011526790.1 |
XM_011528489.2 |
4520 |
Missense Mutation |
AAG,AAT |
K1445N |
XP_011526791.1 |
XM_011528490.2 |
4520 |
Missense Mutation |
AAG,AAT |
K1444N |
XP_011526792.1 |
XM_011528493.2 |
4520 |
Missense Mutation |
AAG,AAT |
K1280N |
XP_011526795.1 |
XM_017027586.1 |
4520 |
Missense Mutation |
AAG,AAT |
K1452N |
XP_016883075.1 |
XM_017027587.1 |
4520 |
Missense Mutation |
AAG,AAT |
K1451N |
XP_016883076.1 |
XM_017027588.1 |
4520 |
Missense Mutation |
AAG,AAT |
K1400N |
XP_016883077.1 |
XM_017027589.1 |
4520 |
Missense Mutation |
AAG,AAT |
K1395N |
XP_016883078.1 |
XM_017027590.1 |
4520 |
Missense Mutation |
AAG,AAT |
K1280N |
XP_016883079.1 |
XM_017027591.1 |
4520 |
Missense Mutation |
AAG,AAT |
K969N |
XP_016883080.1 |
XM_017027592.1 |
4520 |
Intron |
|
|
XP_016883081.1 |
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