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TCCTTAAAGGGAGGTATAGTTAGTC[C/T]CATTATACTCCAGGTAATGATGACA
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 601153 | |||||||||||||||||||||||
Literature Links: |
FHIT 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 |
FHIT - fragile histidine triad | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001166243.2 | 3918 | Intron | NP_001159715.1 | |||
NM_001320899.1 | 3918 | UTR 3 | NP_001307828.1 | |||
NM_001320900.1 | 3918 | UTR 3 | NP_001307829.1 | |||
NM_001320901.1 | 3918 | UTR 3 | NP_001307830.1 | |||
NM_002012.3 | 3918 | Intron | NP_002003.1 | |||
XM_017005880.1 | 3918 | UTR 3 | XP_016861369.1 | |||
XM_017005881.1 | 3918 | UTR 3 | XP_016861370.1 | |||
XM_017005882.1 | 3918 | UTR 3 | XP_016861371.1 | |||
XM_017005883.1 | 3918 | Intron | XP_016861372.1 | |||
XM_017005884.1 | 3918 | Intron | XP_016861373.1 | |||
XM_017005885.1 | 3918 | UTR 3 | XP_016861374.1 | |||
XM_017005886.1 | 3918 | UTR 3 | XP_016861375.1 |