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TCTGACACCAGTTTGGAGGGTGCTG[C/T]ACCCATGGGTCCAACCTAACCAGTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607732 MIM: 611672 | ||||||||||||||||||||
Literature Links: |
SARM1 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 |
SARM1 - sterile alpha and TIR motif containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015077.3 | 2527 | Missense Mutation | GCA,GTA | A,V 719 | NP_055892.2 |
SLC46A1 - solute carrier family 46 member 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001242366.2 | 2527 | UTR 3 | NP_001229295.1 | |||
NM_080669.5 | 2527 | UTR 3 | NP_542400.2 | |||
XM_005277786.3 | 2527 | UTR 3 | XP_005277843.1 | |||
XM_017024110.1 | 2527 | UTR 3 | XP_016879599.1 |