Search Thermo Fisher Scientific
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TCTCCTTGTTGTCTTTCATGAGCTT[G/T]AAGATGGCAGCCAGCTGTTCCTTCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
LOC105274304 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
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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 |
LOC105274304 - uncharacterized LOC105274304 | ||||||
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There are no transcripts associated with this gene. |
MXRA7 - matrix remodeling associated 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001008528.2 | 590 | Missense Mutation | TTA,TTC | L,F 177 | NP_001008528.1 | |
NM_001008529.2 | 590 | Intron | NP_001008529.1 | |||
NM_198530.3 | 590 | Intron | NP_940932.2 | |||
XM_005257382.2 | 590 | Missense Mutation | TTA,TTC | L,F 220 | XP_005257439.1 | |
XM_005257383.2 | 590 | Intron | XP_005257440.1 | |||
XM_005257384.2 | 590 | Intron | XP_005257441.1 | |||
XM_011524830.1 | 590 | Missense Mutation | TTA,TTC | L,F 146 | XP_011523132.1 |