Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCCCCCAGCTTCTTTCTCTTCTGTC[C/T]CCATCTCCTCTTCCTCTTCCTCCTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612914 MIM: 610506 | ||||||||||||||||||||
Literature Links: |
MED29 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 |
MED29 - mediator complex subunit 29 | ||||||
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There are no transcripts associated with this gene. |
PAF1 - PAF1 homolog, Paf1/RNA polymerase II complex component | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256826.1 | 1455 | Missense Mutation | GAG,GGG | E,G 375 | NP_001243755.1 | |
NM_019088.3 | 1455 | Missense Mutation | GAG,GGG | E,G 385 | NP_061961.2 |
SAMD4B - sterile alpha motif domain containing 4B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001303614.1 | 1455 | Intron | NP_001290543.1 | |||
NM_018028.3 | 1455 | Intron | NP_060498.2 | |||
XM_011527057.2 | 1455 | Intron | XP_011525359.1 | |||
XM_011527060.2 | 1455 | Intron | XP_011525362.1 | |||
XM_011527061.2 | 1455 | Intron | XP_011525363.1 | |||
XM_011527062.2 | 1455 | Intron | XP_011525364.1 | |||
XM_011527063.2 | 1455 | Intron | XP_011525365.1 | |||
XM_011527064.2 | 1455 | Intron | XP_011525366.1 | |||
XM_017026918.1 | 1455 | Intron | XP_016882407.1 | |||
XM_017026919.1 | 1455 | Intron | XP_016882408.1 | |||
XM_017026920.1 | 1455 | Intron | XP_016882409.1 | |||
XM_017026921.1 | 1455 | Intron | XP_016882410.1 | |||
XM_017026922.1 | 1455 | Intron | XP_016882411.1 | |||
XM_017026923.1 | 1455 | Intron | XP_016882412.1 |