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TCCTGCAGCTACTGCCTTCCTCATC[A/C]ACAAAGTGCCCCTTCCTGTTGACAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606531 | ||||||||||||||||||||
Literature Links: |
C5orf46 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 |
C5orf46 - chromosome 5 open reading frame 46 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_206966.2 | 166 | Intron | NP_996849.2 | |||
XM_005268446.3 | 166 | Intron | XP_005268503.2 | |||
XM_017009459.1 | 166 | Intron | XP_016864948.1 |
SCGB3A2 - secretoglobin family 3A member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_054023.4 | 166 | Missense Mutation | AAC,CAC | N,H 25 | NP_473364.1 |