Product Details
- SNP ID
-
rs149678283
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.12:57254926 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CAGCCACAATGGTGTACAAGGCAGC[A/G]AGGTCCGAGTGGCGGCCATTCTCAG
- Phenotype
-
MIM: 615521
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
R3HDM2
PubMed Links
Gene Details
- Gene
- R3HDM2
- Gene Name
- R3H domain containing 2
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
XM_005268725.3 |
3088 |
Silent Mutation |
CTC,CTT |
L926L |
XP_005268782.1 |
XM_011538031.1 |
3088 |
Silent Mutation |
CTC,CTT |
L1005L |
XP_011536333.1 |
XM_011538033.1 |
3088 |
Silent Mutation |
CTC,CTT |
L1000L |
XP_011536335.1 |
XM_011538035.1 |
3088 |
Silent Mutation |
CTC,CTT |
L991L |
XP_011536337.1 |
XM_011538036.1 |
3088 |
Silent Mutation |
CTC,CTT |
L989L |
XP_011536338.1 |
XM_011538037.1 |
3088 |
Silent Mutation |
CTC,CTT |
L983L |
XP_011536339.1 |
XM_011538038.1 |
3088 |
Silent Mutation |
CTC,CTT |
L973L |
XP_011536340.1 |
XM_011538039.1 |
3088 |
Silent Mutation |
CTC,CTT |
L971L |
XP_011536341.1 |
XM_011538040.1 |
3088 |
Silent Mutation |
CTC,CTT |
L966L |
XP_011536342.1 |
XM_011538042.2 |
3088 |
Silent Mutation |
CTC,CTT |
L1023L |
XP_011536344.1 |
XM_017018998.1 |
3088 |
Silent Mutation |
CTC,CTT |
L997L |
XP_016874487.1 |
XM_017018999.1 |
3088 |
Silent Mutation |
CTC,CTT |
L1023L |
XP_016874488.1 |
XM_017019000.1 |
3088 |
Silent Mutation |
CTC,CTT |
L968L |
XP_016874489.1 |
XM_017019001.1 |
3088 |
Silent Mutation |
CTC,CTT |
L1015L |
XP_016874490.1 |
XM_017019002.1 |
3088 |
Silent Mutation |
CTC,CTT |
L958L |
XP_016874491.1 |
XM_017019003.1 |
3088 |
Silent Mutation |
CTC,CTT |
L950L |
XP_016874492.1 |
XM_017019004.1 |
3088 |
Silent Mutation |
CTC,CTT |
L948L |
XP_016874493.1 |
XM_017019005.1 |
3088 |
Silent Mutation |
CTC,CTT |
L992L |
XP_016874494.1 |
XM_017019006.1 |
3088 |
Silent Mutation |
CTC,CTT |
L992L |
XP_016874495.1 |
XM_017019007.1 |
3088 |
Silent Mutation |
CTC,CTT |
L992L |
XP_016874496.1 |
XM_017019008.1 |
3088 |
Silent Mutation |
CTC,CTT |
L939L |
XP_016874497.1 |
XM_017019009.1 |
3088 |
Silent Mutation |
CTC,CTT |
L934L |
XP_016874498.1 |
XM_017019010.1 |
3088 |
Intron |
|
|
XP_016874499.1 |
XM_017019011.1 |
3088 |
Silent Mutation |
CTC,CTT |
L982L |
XP_016874500.1 |
XM_017019012.1 |
3088 |
Silent Mutation |
CTC,CTT |
L928L |
XP_016874501.1 |
XM_017019013.1 |
3088 |
Intron |
|
|
XP_016874502.1 |
XM_017019014.1 |
3088 |
Silent Mutation |
CTC,CTT |
L974L |
XP_016874503.1 |
XM_017019015.1 |
3088 |
Silent Mutation |
CTC,CTT |
L962L |
XP_016874504.1 |
XM_017019016.1 |
3088 |
Silent Mutation |
CTC,CTT |
L960L |
XP_016874505.1 |
XM_017019017.1 |
3088 |
Intron |
|
|
XP_016874506.1 |
XM_017019018.1 |
3088 |
Silent Mutation |
CTC,CTT |
L958L |
XP_016874507.1 |
XM_017019019.1 |
3088 |
Silent Mutation |
CTC,CTT |
L948L |
XP_016874508.1 |
XM_017019020.1 |
3088 |
Silent Mutation |
CTC,CTT |
L896L |
XP_016874509.1 |
XM_017019021.1 |
3088 |
Silent Mutation |
CTC,CTT |
L942L |
XP_016874510.1 |
XM_017019022.1 |
3088 |
Intron |
|
|
XP_016874511.1 |
XM_017019023.1 |
3088 |
Silent Mutation |
CTC,CTT |
L942L |
XP_016874512.1 |
XM_017019024.1 |
3088 |
Silent Mutation |
CTC,CTT |
L942L |
XP_016874513.1 |
XM_017019025.1 |
3088 |
Silent Mutation |
CTC,CTT |
L938L |
XP_016874514.1 |
XM_017019026.1 |
3088 |
Silent Mutation |
CTC,CTT |
L916L |
XP_016874515.1 |
XM_017019027.1 |
3088 |
Silent Mutation |
CTC,CTT |
L908L |
XP_016874516.1 |
XM_017019028.1 |
3088 |
Silent Mutation |
CTC,CTT |
L908L |
XP_016874517.1 |
XM_017019029.1 |
3088 |
Silent Mutation |
CTC,CTT |
L888L |
XP_016874518.1 |
XM_017019030.1 |
3088 |
Silent Mutation |
CTC,CTT |
L653L |
XP_016874519.1 |
XM_017019031.1 |
3088 |
Silent Mutation |
CTC,CTT |
L621L |
XP_016874520.1 |
XM_017019032.1 |
3088 |
Silent Mutation |
CTC,CTT |
L587L |
XP_016874521.1 |
XM_017019033.1 |
3088 |
Silent Mutation |
CTC,CTT |
L587L |
XP_016874522.1 |
- Gene
- STAC3
- Gene Name
- SH3 and cysteine rich domain 3
There are no transcripts associated with this gene.
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