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CTCGTAGGTGGTGGCGGGTGGCTTG[C/T]GGTCGAAGAGCTCGTCGCGGCTGTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
BEGAIN PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
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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 |
BEGAIN - brain enriched guanylate kinase associated | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001159531.1 | 1295 | Missense Mutation | CAC,CGC | H,R 336 | NP_001153003.1 | |
NM_020836.3 | 1295 | Missense Mutation | CAC,CGC | H,R 336 | NP_065887.1 | |
XM_005267919.3 | 1295 | Missense Mutation | CAC,CGC | H,R 349 | XP_005267976.1 | |
XM_005267920.4 | 1295 | Missense Mutation | CAC,CGC | H,R 348 | XP_005267977.1 | |
XM_005267921.3 | 1295 | Missense Mutation | CAC,CGC | H,R 336 | XP_005267978.1 | |
XM_011537031.1 | 1295 | Missense Mutation | CAC,CGC | H,R 355 | XP_011535333.1 | |
XM_017021521.1 | 1295 | Missense Mutation | CAC,CGC | H,R 336 | XP_016877010.1 | |
XM_017021522.1 | 1295 | Missense Mutation | CAC,CGC | H,R 327 | XP_016877011.1 |
WDR25 - WD repeat domain 25 | ||||||
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There are no transcripts associated with this gene. |