Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCCAGCAACAACGCATGGCCGCTAT[A/G]GGGACCGACAAGGAGCTGAGCGACC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600480 | ||||||||||||||||||||
Literature Links: |
LOC145783 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | 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 |
LOC145783 - uncharacterized LOC145783 | ||||||
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There are no transcripts associated with this gene. |
TCF12 - transcription factor 12 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001306219.2 | 174 | Intron | NP_001293148.1 | |||
NM_001306220.2 | 174 | Intron | NP_001293149.1 | |||
NM_001322151.1 | 174 | Missense Mutation | ATA,ATG | I,M 11 | NP_001309080.1 | |
NM_001322152.1 | 174 | Missense Mutation | ATA,ATG | I,M 11 | NP_001309081.1 | |
NM_001322154.1 | 174 | UTR 5 | NP_001309083.1 | |||
NM_001322156.1 | 174 | UTR 5 | NP_001309085.1 | |||
NM_001322157.1 | 174 | Missense Mutation | ATA,ATG | I,M 11 | NP_001309086.1 | |
NM_001322158.1 | 174 | UTR 5 | NP_001309087.1 | |||
NM_001322159.1 | 174 | Missense Mutation | ATA,ATG | I,M 11 | NP_001309088.1 | |
NM_001322161.1 | 174 | Missense Mutation | ATA,ATG | I,M 11 | NP_001309090.1 | |
NM_001322162.1 | 174 | Missense Mutation | ATA,ATG | I,M 11 | NP_001309091.1 | |
NM_001322164.1 | 174 | Missense Mutation | ATA,ATG | I,M 11 | NP_001309093.1 | |
NM_001322165.1 | 174 | Missense Mutation | ATA,ATG | I,M 11 | NP_001309094.1 | |
NM_003205.3 | 174 | Missense Mutation | ATA,ATG | I,M 11 | NP_003196.1 | |
NM_207036.1 | 174 | Missense Mutation | ATA,ATG | I,M 11 | NP_996919.1 | |
NM_207037.1 | 174 | Missense Mutation | ATA,ATG | I,M 11 | NP_996920.1 | |
NM_207038.1 | 174 | Missense Mutation | ATA,ATG | I,M 11 | NP_996921.1 | |
NM_207040.1 | 174 | Intron | NP_996923.1 | |||
XM_011521959.2 | 174 | Missense Mutation | ATA,ATG | I,M 11 | XP_011520261.1 | |
XM_011521960.2 | 174 | Missense Mutation | ATA,ATG | I,M 11 | XP_011520262.1 | |
XM_011521961.2 | 174 | Missense Mutation | ATA,ATG | I,M 11 | XP_011520263.1 | |
XM_011521962.2 | 174 | Missense Mutation | ATA,ATG | I,M 11 | XP_011520264.1 | |
XM_011521963.2 | 174 | Missense Mutation | ATA,ATG | I,M 11 | XP_011520265.1 | |
XM_011521965.1 | 174 | UTR 5 | XP_011520267.1 | |||
XM_011521966.2 | 174 | Intron | XP_011520268.1 | |||
XM_011521967.1 | 174 | UTR 5 | XP_011520269.1 | |||
XM_011521969.1 | 174 | Intron | XP_011520271.1 | |||
XM_017022520.1 | 174 | Missense Mutation | ATA,ATG | I,M 11 | XP_016878009.1 |