Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TATTCCAGTAATGGTGGATGAAGTT[G/T]TTCATTGTTTGTCACCACAAAAAGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 611271 | ||||||||||||||||||||
Literature Links: |
KIF18A PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
KIF18A - kinesin family member 18A | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
METTL15 - methyltransferase like 15 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001113528.1 | 696 | Missense Mutation | GTT,TTT | V,F 81 | NP_001107000.1 | |
NM_001297775.1 | 696 | Missense Mutation | GTT,TTT | V,F 81 | NP_001284704.1 | |
NM_152636.2 | 696 | Missense Mutation | GTT,TTT | V,F 81 | NP_689849.2 | |
XM_011519935.2 | 696 | UTR 5 | XP_011518237.1 | |||
XM_011519937.2 | 696 | Intron | XP_011518239.1 | |||
XM_011519940.2 | 696 | Missense Mutation | GTT,TTT | V,F 81 | XP_011518242.1 | |
XM_011519941.2 | 696 | Missense Mutation | GTT,TTT | V,F 81 | XP_011518243.1 | |
XM_017017297.1 | 696 | Missense Mutation | GTT,TTT | V,F 81 | XP_016872786.1 | |
XM_017017298.1 | 696 | UTR 5 | XP_016872787.1 | |||
XM_017017299.1 | 696 | Intron | XP_016872788.1 | |||
XM_017017300.1 | 696 | UTR 5 | XP_016872789.1 | |||
XM_017017301.1 | 696 | Missense Mutation | GTT,TTT | V,F 81 | XP_016872790.1 | |
XM_017017302.1 | 696 | Intron | XP_016872791.1 | |||
XM_017017303.1 | 696 | UTR 5 | XP_016872792.1 |