Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCTCACCTGCTGCAGGACGCGGGCA[C/G]GGGAGGCCAAGGCAGCGCTGTGCTC
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
SSUH2 PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR - Not Available | |||||
AMR - Not Available |
SSUH2 - ssu-2 homolog (C. elegans) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256748.1 | 969 | Missense Mutation | CCT,CGT | P,R 321 | NP_001243677.1 | |
NM_001256749.1 | 969 | Missense Mutation | CCT,CGT | P,R 248 | NP_001243678.1 | |
NM_015931.2 | 969 | Missense Mutation | CCT,CGT | P,R 299 | NP_057015.1 | |
XM_011533774.1 | 969 | Missense Mutation | CCT,CGT | P,R 504 | XP_011532076.1 | |
XM_017006510.1 | 969 | Missense Mutation | CCT,CGT | P,R 512 | XP_016861999.1 | |
XM_017006511.1 | 969 | Missense Mutation | CCT,CGT | P,R 504 | XP_016862000.1 | |
XM_017006512.1 | 969 | Missense Mutation | CCT,CGT | P,R 504 | XP_016862001.1 | |
XM_017006513.1 | 969 | Missense Mutation | CCT,CGT | P,R 504 | XP_016862002.1 | |
XM_017006514.1 | 969 | Missense Mutation | CCT,CGT | P,R 504 | XP_016862003.1 | |
XM_017006515.1 | 969 | Missense Mutation | CCT,CGT | P,R 504 | XP_016862004.1 | |
XM_017006516.1 | 969 | Missense Mutation | CCT,CGT | P,R 504 | XP_016862005.1 | |
XM_017006517.1 | 969 | Missense Mutation | CCT,CGT | P,R 504 | XP_016862006.1 | |
XM_017006518.1 | 969 | Missense Mutation | CCT,CGT | P,R 497 | XP_016862007.1 | |
XM_017006519.1 | 969 | Missense Mutation | CCT,CGT | P,R 494 | XP_016862008.1 | |
XM_017006520.1 | 969 | Missense Mutation | CCT,CGT | P,R 490 | XP_016862009.1 | |
XM_017006521.1 | 969 | Missense Mutation | CCT,CGT | P,R 472 | XP_016862010.1 | |
XM_017006522.1 | 969 | Missense Mutation | CCT,CGT | P,R 472 | XP_016862011.1 | |
XM_017006523.1 | 969 | Missense Mutation | CCT,CGT | P,R 472 | XP_016862012.1 | |
XM_017006524.1 | 969 | Missense Mutation | CCT,CGT | P,R 463 | XP_016862013.1 | |
XM_017006525.1 | 969 | Missense Mutation | CCT,CGT | P,R 462 | XP_016862014.1 | |
XM_017006526.1 | 969 | Missense Mutation | CCT,CGT | P,R 462 | XP_016862015.1 | |
XM_017006527.1 | 969 | Missense Mutation | CCT,CGT | P,R 436 | XP_016862016.1 | |
XM_017006528.1 | 969 | Missense Mutation | CCT,CGT | P,R 436 | XP_016862017.1 | |
XM_017006529.1 | 969 | Missense Mutation | CCT,CGT | P,R 436 | XP_016862018.1 | |
XM_017006530.1 | 969 | Missense Mutation | CCT,CGT | P,R 436 | XP_016862019.1 | |
XM_017006531.1 | 969 | Missense Mutation | CCT,CGT | P,R 436 | XP_016862020.1 | |
XM_017006532.1 | 969 | Intron | XP_016862021.1 | |||
XM_017006533.1 | 969 | Missense Mutation | CCT,CGT | P,R 429 | XP_016862022.1 | |
XM_017006534.1 | 969 | Missense Mutation | CCT,CGT | P,R 411 | 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 | P,R 299 | XP_016862027.1 | |
XM_017006539.1 | 969 | Missense Mutation | CCT,CGT | P,R 299 | XP_016862028.1 | |
XM_017006540.1 | 969 | Missense Mutation | CCT,CGT | P,R 299 | XP_016862029.1 | |
XM_017006541.1 | 969 | Missense Mutation | CCT,CGT | P,R 299 | XP_016862030.1 | |
XM_017006542.1 | 969 | Missense Mutation | CCT,CGT | P,R 299 | XP_016862031.1 |