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GCCATGGTCTGTCTCTTCCTGAAGT[A/G]CATGCTCCTTCCGTTAGACCGTGCT
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 608435 | |||||||||||||||||||||||
Literature Links: |
MRAS 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 |
MRAS - muscle RAS oncogene homolog | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001085049.2 | Intron | NP_001078518.1 | ||||
NM_001252090.1 | Intron | NP_001239019.1 | ||||
NM_001252091.1 | Intron | NP_001239020.1 | ||||
NM_001252092.1 | Intron | NP_001239021.1 | ||||
NM_001252093.1 | Intron | NP_001239022.1 | ||||
NM_012219.4 | Intron | NP_036351.3 | ||||
XM_005247228.1 | Intron | XP_005247285.1 | ||||
XM_005247229.2 | Intron | XP_005247286.1 | ||||
XM_017005887.1 | Intron | XP_016861376.1 |