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TCCCTGTCCCCCCAGAAAAGAAAAG[A/G]TGCAGCCACCAGAAAAAGAAACTCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612085 | ||||||||||||||||||||
Literature Links: |
RASL12 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 |
RASL12 - RAS like family 12 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001307930.1 | 495 | Intron | NP_001294859.1 | |||
NM_016563.3 | 495 | Intron | NP_057647.1 | |||
XM_005254434.4 | 495 | Intron | XP_005254491.1 | |||
XM_011521660.2 | 495 | Intron | XP_011519962.1 | |||
XM_017022296.1 | 495 | Intron | XP_016877785.1 |
SLC51B - solute carrier family 51 beta subunit | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_178859.3 | 495 | Missense Mutation | ATG,GTG | M,V 67 | NP_849190.2 | |
XM_005254159.4 | 495 | Missense Mutation | ATG,GTG | M,V 67 | XP_005254216.1 |