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AGTTACAAGAGTTATATAGGTACTT[C/T]AGTATCTTCATTATTTTTCGTGGAT
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 600586 | |||||||||||||||||||||||
Literature Links: |
ECT2 PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
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 |
ECT2 - epithelial cell transforming 2 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001258315.1 | Intron | NP_001245244.1 | ||||
NM_001258316.1 | Intron | NP_001245245.1 | ||||
NM_018098.5 | Intron | NP_060568.3 | ||||
XM_005247176.1 | Intron | XP_005247233.1 | ||||
XM_006713523.3 | Intron | XP_006713586.1 | ||||
XM_006713524.3 | Intron | XP_006713587.1 | ||||
XM_011512514.2 | Intron | XP_011510816.1 | ||||
XM_011512515.2 | Intron | XP_011510817.1 | ||||
XM_011512516.1 | Intron | XP_011510818.1 | ||||
XM_017005830.1 | Intron | XP_016861319.1 | ||||
XM_017005831.1 | Intron | XP_016861320.1 | ||||
XM_017005832.1 | Intron | XP_016861321.1 | ||||
XM_017005833.1 | Intron | XP_016861322.1 | ||||
XM_017005834.1 | Intron | XP_016861323.1 | ||||
XM_017005835.1 | Intron | XP_016861324.1 | ||||
XM_017005836.1 | Intron | XP_016861325.1 | ||||
XM_017005837.1 | Intron | XP_016861326.1 | ||||
XM_017005838.1 | Intron | XP_016861327.1 |