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AGCTGTTCAAGCTCCAGAACAATTG[C/T]TGCATATCTCCGCTGAAATTCAATG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
2 submissions
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Phenotype: |
MIM: 609375 | ||||||||||||||||||||
Literature Links: |
LIN9 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 |
LIN9 - lin-9 DREAM MuvB core complex component | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001270409.1 | 1187 | Missense Mutation | ACA,GCA | T,A 371 | NP_001257338.1 | |
NM_001270410.1 | 1187 | Missense Mutation | ACA,GCA | T,A 338 | NP_001257339.1 | |
NM_173083.3 | 1187 | Missense Mutation | ACA,GCA | T,A 406 | NP_775106.2 | |
XM_005273102.3 | 1187 | Missense Mutation | ACA,GCA | T,A 463 | XP_005273159.1 | |
XM_006711766.2 | 1187 | Missense Mutation | ACA,GCA | T,A 372 | XP_006711829.2 | |
XM_006711767.3 | 1187 | Missense Mutation | ACA,GCA | T,A 338 | XP_006711830.1 | |
XM_011544173.2 | 1187 | Intron | XP_011542475.1 | |||
XM_017001084.1 | 1187 | Missense Mutation | ACA,GCA | T,A 394 | XP_016856573.1 |