Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGAAACTCTACGAAAACAAGTCATT[G/T]CTTTTCCTGGGCTGTGGCTGGACTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616587 MIM: 182180 | ||||||||||||||||||||
Literature Links: |
FAM118B 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 |
FAM118B - family with sequence similarity 118 member B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_024556.3 | 846 | Missense Mutation | TTG,TTT | L,F 244 | NP_078832.1 | |
XM_005271665.3 | 846 | Missense Mutation | TTG,TTT | L,F 244 | XP_005271722.1 | |
XM_011542977.2 | 846 | Missense Mutation | TTG,TTT | L,F 244 | XP_011541279.1 | |
XM_011542978.2 | 846 | Missense Mutation | TTG,TTT | L,F 89 | XP_011541280.1 | |
XM_017018285.1 | 846 | Missense Mutation | TTG,TTT | L,F 244 | XP_016873774.1 | |
XM_017018286.1 | 846 | Missense Mutation | TTG,TTT | L,F 89 | XP_016873775.1 |
SRPRA - SRP receptor alpha subunit | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001177842.1 | 846 | Intron | NP_001171313.1 | |||
NM_003139.3 | 846 | Intron | NP_003130.2 | |||
XM_017018179.1 | 846 | UTR 3 | XP_016873668.1 |