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TCCCTTATAAGAAACCTTGTCCTTA[C/T]GGGTCGAGTGCCCCATGGGATAATG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614311 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC105372585 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
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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LOC105372585 - translation initiation factor IF-2-like | ||||||
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There are no transcripts associated with this gene. |
SYNDIG1 - synapse differentiation inducing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001323606.1 | Intron | NP_001310535.1 | ||||
NM_001323607.1 | Intron | NP_001310536.1 | ||||
NM_024893.2 | Intron | NP_079169.1 | ||||
XM_011529347.2 | Intron | XP_011527649.1 | ||||
XM_011529348.2 | Intron | XP_011527650.1 | ||||
XM_011529349.2 | Intron | XP_011527651.1 | ||||
XM_011529350.1 | Intron | XP_011527652.1 | ||||
XM_011529351.1 | Intron | XP_011527653.1 | ||||
XM_011529352.2 | Intron | XP_011527654.1 | ||||
XM_011529353.2 | Intron | XP_011527655.1 | ||||
XM_011529354.2 | Intron | XP_011527656.1 | ||||
XM_011529356.2 | Intron | XP_011527658.1 | ||||
XM_011529358.2 | Intron | XP_011527660.1 | ||||
XM_017028064.1 | Intron | XP_016883553.1 | ||||
XM_017028065.1 | Intron | XP_016883554.1 | ||||
XM_017028066.1 | Intron | XP_016883555.1 | ||||
XM_017028067.1 | Intron | XP_016883556.1 | ||||
XM_017028068.1 | Intron | XP_016883557.1 | ||||
XM_017028069.1 | Intron | XP_016883558.1 |