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TCAGGGGATAGTGAAGTTTACCAAC[C/T]GGGTGAGTACAAAAGACTGGGGTTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600439 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SSBP1 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
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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SSBP1 - single stranded DNA binding protein 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256510.1 | 485 | Missense Mutation | CCG,CTG | P,L 75 | NP_001243439.1 | |
NM_001256511.1 | 485 | Missense Mutation | CCG,CTG | P,L 75 | NP_001243440.1 | |
NM_001256512.1 | 485 | Missense Mutation | CCG,CTG | P,L 75 | NP_001243441.1 | |
NM_001256513.1 | 485 | Intron | NP_001243442.1 | |||
NM_003143.2 | 485 | Intron | NP_003134.1 | |||
XM_005250048.4 | 485 | Missense Mutation | CCG,CTG | P,L 75 | XP_005250105.1 | |
XM_005250049.4 | 485 | Missense Mutation | CCG,CTG | P,L 75 | XP_005250106.1 | |
XM_005250050.4 | 485 | Missense Mutation | CCG,CTG | P,L 75 | XP_005250107.1 | |
XM_005250051.4 | 485 | Missense Mutation | CCG,CTG | P,L 75 | XP_005250108.1 |
WEE2-AS1 - WEE2 antisense RNA 1 | ||||||
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There are no transcripts associated with this gene. |