Product Details
- SNP ID
-
rs149593163
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.3:8623568 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GCTCACCTGCTGCAGGACGCGGGCA[C/G]GGGAGGCCAAGGCAGCGCTGTGCTC
- Phenotype
-
- Polymorphism
- C/G, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
SSUH2
PubMed Links
Gene Details
- Gene
- SSUH2
- Gene Name
- ssu-2 homolog (C. elegans)
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001256748.1 |
969 |
Missense Mutation |
CCT,CGT |
P321R |
NP_001243677.1 |
NM_001256749.1 |
969 |
Missense Mutation |
CCT,CGT |
P248R |
NP_001243678.1 |
NM_015931.2 |
969 |
Missense Mutation |
CCT,CGT |
P299R |
NP_057015.1 |
XM_011533774.1 |
969 |
Missense Mutation |
CCT,CGT |
P504R |
XP_011532076.1 |
XM_017006510.1 |
969 |
Missense Mutation |
CCT,CGT |
P512R |
XP_016861999.1 |
XM_017006511.1 |
969 |
Missense Mutation |
CCT,CGT |
P504R |
XP_016862000.1 |
XM_017006512.1 |
969 |
Missense Mutation |
CCT,CGT |
P504R |
XP_016862001.1 |
XM_017006513.1 |
969 |
Missense Mutation |
CCT,CGT |
P504R |
XP_016862002.1 |
XM_017006514.1 |
969 |
Missense Mutation |
CCT,CGT |
P504R |
XP_016862003.1 |
XM_017006515.1 |
969 |
Missense Mutation |
CCT,CGT |
P504R |
XP_016862004.1 |
XM_017006516.1 |
969 |
Missense Mutation |
CCT,CGT |
P504R |
XP_016862005.1 |
XM_017006517.1 |
969 |
Missense Mutation |
CCT,CGT |
P504R |
XP_016862006.1 |
XM_017006518.1 |
969 |
Missense Mutation |
CCT,CGT |
P497R |
XP_016862007.1 |
XM_017006519.1 |
969 |
Missense Mutation |
CCT,CGT |
P494R |
XP_016862008.1 |
XM_017006520.1 |
969 |
Missense Mutation |
CCT,CGT |
P490R |
XP_016862009.1 |
XM_017006521.1 |
969 |
Missense Mutation |
CCT,CGT |
P472R |
XP_016862010.1 |
XM_017006522.1 |
969 |
Missense Mutation |
CCT,CGT |
P472R |
XP_016862011.1 |
XM_017006523.1 |
969 |
Missense Mutation |
CCT,CGT |
P472R |
XP_016862012.1 |
XM_017006524.1 |
969 |
Missense Mutation |
CCT,CGT |
P463R |
XP_016862013.1 |
XM_017006525.1 |
969 |
Missense Mutation |
CCT,CGT |
P462R |
XP_016862014.1 |
XM_017006526.1 |
969 |
Missense Mutation |
CCT,CGT |
P462R |
XP_016862015.1 |
XM_017006527.1 |
969 |
Missense Mutation |
CCT,CGT |
P436R |
XP_016862016.1 |
XM_017006528.1 |
969 |
Missense Mutation |
CCT,CGT |
P436R |
XP_016862017.1 |
XM_017006529.1 |
969 |
Missense Mutation |
CCT,CGT |
P436R |
XP_016862018.1 |
XM_017006530.1 |
969 |
Missense Mutation |
CCT,CGT |
P436R |
XP_016862019.1 |
XM_017006531.1 |
969 |
Missense Mutation |
CCT,CGT |
P436R |
XP_016862020.1 |
XM_017006532.1 |
969 |
Intron |
|
|
XP_016862021.1 |
XM_017006533.1 |
969 |
Missense Mutation |
CCT,CGT |
P429R |
XP_016862022.1 |
XM_017006534.1 |
969 |
Missense Mutation |
CCT,CGT |
P411R |
XP_016862023.1 |
XM_017006535.1 |
969 |
Intron |
|
|
XP_016862024.1 |
XM_017006536.1 |
969 |
Intron |
|
|
XP_016862025.1 |
XM_017006537.1 |
969 |
Intron |
|
|
XP_016862026.1 |
XM_017006538.1 |
969 |
Missense Mutation |
CCT,CGT |
P299R |
XP_016862027.1 |
XM_017006539.1 |
969 |
Missense Mutation |
CCT,CGT |
P299R |
XP_016862028.1 |
XM_017006540.1 |
969 |
Missense Mutation |
CCT,CGT |
P299R |
XP_016862029.1 |
XM_017006541.1 |
969 |
Missense Mutation |
CCT,CGT |
P299R |
XP_016862030.1 |
XM_017006542.1 |
969 |
Missense Mutation |
CCT,CGT |
P299R |
XP_016862031.1 |
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