Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCCTCCGCGGCTGGGTCCCCCGGTG[A/G]CCTCACCAGCCTCCAGCAGCAGAAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604913 MIM: 609927 | ||||||||||||||||||||
Literature Links: |
CNOT7 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 |
CNOT7 - CCR4-NOT transcription complex subunit 7 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001322087.1 | 380 | Intron | NP_001309016.1 | |||
NM_001322088.1 | 380 | Intron | NP_001309017.1 | |||
NM_001322089.1 | 380 | Intron | NP_001309018.1 | |||
NM_001322090.1 | 380 | Intron | NP_001309019.1 | |||
NM_001322091.1 | 380 | Intron | NP_001309020.1 | |||
NM_001322092.1 | 380 | Intron | NP_001309021.1 | |||
NM_001322093.1 | 380 | Intron | NP_001309022.1 | |||
NM_001322094.1 | 380 | Intron | NP_001309023.1 | |||
NM_001322095.1 | 380 | Intron | NP_001309024.1 | |||
NM_001322096.1 | 380 | Intron | NP_001309025.1 | |||
NM_001322097.1 | 380 | Intron | NP_001309026.1 | |||
NM_001322098.1 | 380 | Intron | NP_001309027.1 | |||
NM_001322099.1 | 380 | Intron | NP_001309028.1 | |||
NM_001322100.1 | 380 | Intron | NP_001309029.1 | |||
NM_013354.6 | 380 | Intron | NP_037486.2 | |||
NM_054026.3 | 380 | Intron | NP_473367.2 | |||
XM_005273481.2 | 380 | Intron | XP_005273538.1 |
VPS37A - VPS37A, ESCRT-I subunit | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145152.1 | 380 | Missense Mutation | GAC,GGC | D,G 21 | NP_001138624.1 | |
NM_152415.2 | 380 | Missense Mutation | GAC,GGC | D,G 21 | NP_689628.2 | |
XM_005273400.2 | 380 | UTR 5 | XP_005273457.1 | |||
XM_005273401.2 | 380 | UTR 5 | XP_005273458.1 | |||
XM_006716286.1 | 380 | Missense Mutation | GAC,GGC | D,G 21 | XP_006716349.1 | |
XM_017013021.1 | 380 | Missense Mutation | GAC,GGC | D,G 21 | XP_016868510.1 | |
XM_017013022.1 | 380 | Missense Mutation | GAC,GGC | D,G 21 | XP_016868511.1 | |
XM_017013023.1 | 380 | UTR 5 | XP_016868512.1 | |||
XM_017013024.1 | 380 | UTR 5 | XP_016868513.1 | |||
XM_017013025.1 | 380 | UTR 5 | XP_016868514.1 | |||
XM_017013026.1 | 380 | Intron | XP_016868515.1 |