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GTGTTACACACCAATGATTGTTGCC[A/G]CTGATTTTGTCAAATCTATAAAAGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606821 | ||||||||||||||||||||
Literature Links: |
BCAP29 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 |
BCAP29 - B-cell receptor-associated protein 29 | ||||||
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There are no transcripts associated with this gene. |
COG5 - component of oligomeric golgi complex 5 | ||||||
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There are no transcripts associated with this gene. |
DUS4L - dihydrouridine synthase 4 like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001270419.1 | 291 | Missense Mutation | ACT,GCT | T,A 62 | NP_001257348.1 | |
NM_181581.2 | 291 | Missense Mutation | ACT,GCT | T,A 62 | NP_853559.1 | |
XM_005250125.4 | 291 | Missense Mutation | ACT,GCT | T,A 62 | XP_005250182.1 | |
XM_006715844.2 | 291 | Intron | XP_006715907.1 | |||
XM_006715845.3 | 291 | Intron | XP_006715908.1 | |||
XM_011515766.2 | 291 | Missense Mutation | ACT,GCT | T,A 62 | XP_011514068.1 | |
XM_011515767.2 | 291 | Missense Mutation | ACT,GCT | T,A 62 | XP_011514069.1 | |
XM_017011708.1 | 291 | Missense Mutation | ACT,GCT | T,A 62 | XP_016867197.1 | |
XM_017011709.1 | 291 | Missense Mutation | ACT,GCT | T,A 58 | XP_016867198.1 | |
XM_017011710.1 | 291 | Missense Mutation | ACT,GCT | T,A 58 | XP_016867199.1 | |
XM_017011711.1 | 291 | Missense Mutation | ACT,GCT | T,A 58 | XP_016867200.1 | |
XM_017011712.1 | 291 | Missense Mutation | ACT,GCT | T,A 58 | XP_016867201.1 | |
XM_017011713.1 | 291 | Missense Mutation | ACT,GCT | T,A 58 | XP_016867202.1 |