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Search Thermo Fisher Scientific
CTGATAAAAATGGCATGGACTTCTA[A/T]TCGTCTGTCCGTTTTCTGCAGCAGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
2 submissions
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Phenotype: |
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Literature Links: |
BRINP3 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 |
BRINP3 - BMP/retinoic acid inducible neural specific 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001317188.1 | 2097 | Missense Mutation | ATA,TTA | I,L 406 | NP_001304117.1 | |
NM_199051.2 | 2097 | Missense Mutation | ATA,TTA | I,L 508 | NP_950252.1 | |
XM_011509472.2 | 2097 | Missense Mutation | ATA,TTA | I,L 478 | XP_011507774.1 | |
XM_011509475.2 | 2097 | Missense Mutation | ATA,TTA | I,L 465 | XP_011507777.1 | |
XM_011509476.2 | 2097 | Missense Mutation | ATA,TTA | I,L 406 | XP_011507778.1 | |
XM_017001125.1 | 2097 | Missense Mutation | ATA,TTA | I,L 508 | XP_016856614.1 | |
XM_017001126.1 | 2097 | Missense Mutation | ATA,TTA | I,L 508 | XP_016856615.1 | |
XM_017001127.1 | 2097 | Missense Mutation | ATA,TTA | I,L 478 | XP_016856616.1 | |
XM_017001128.1 | 2097 | Missense Mutation | ATA,TTA | I,L 478 | XP_016856617.1 | |
XM_017001129.1 | 2097 | Missense Mutation | ATA,TTA | I,L 406 | XP_016856618.1 | |
XM_017001130.1 | 2097 | Missense Mutation | ATA,TTA | I,L 406 | XP_016856619.1 | |
XM_017001131.1 | 2097 | Missense Mutation | ATA,TTA | I,L 215 | XP_016856620.1 | |
XM_017001132.1 | 2097 | Intron | XP_016856621.1 | |||
XM_017001133.1 | 2097 | Intron | XP_016856622.1 |