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AGCCCTTCACAGCCTTCAGCTTGTC[A/G]CTCTCGAAGTTCACCACCAGCTTGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 190196 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TGM2 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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TGM2 - transglutaminase 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001323316.1 | 2224 | Silent Mutation | AGC,AGT | S,S 670 | NP_001310245.1 | |
NM_001323317.1 | 2224 | Silent Mutation | AGC,AGT | S,S 589 | NP_001310246.1 | |
NM_001323318.1 | 2224 | Silent Mutation | AGC,AGT | S,S 610 | NP_001310247.1 | |
NM_004613.3 | 2224 | Silent Mutation | AGC,AGT | S,S 670 | NP_004604.2 | |
NM_198951.2 | 2224 | Intron | NP_945189.1 | |||
XM_011529028.1 | 2224 | Silent Mutation | AGC,AGT | S,S 670 | XP_011527330.1 |