Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTTCCTCACGGATCCTGAAGGGGGG[C/T]TCTCTGCAGAGCGACCACCCCATCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 300409 | ||||||||||||||||||||
Literature Links: |
MORF4L2 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 |
MORF4L2 - mortality factor 4 like 2 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001142418.1 | 701 | Missense Mutation | AAC,AGC | N,S 66 | NP_001135890.1 | |
NM_001142419.1 | 701 | Missense Mutation | AAC,AGC | N,S 66 | NP_001135891.1 | |
NM_001142420.1 | 701 | Missense Mutation | AAC,AGC | N,S 66 | NP_001135892.1 | |
NM_001142421.1 | 701 | Missense Mutation | AAC,AGC | N,S 66 | NP_001135893.1 | |
NM_001142422.1 | 701 | Missense Mutation | AAC,AGC | N,S 66 | NP_001135894.1 | |
NM_001142423.1 | 701 | Missense Mutation | AAC,AGC | N,S 66 | NP_001135895.1 | |
NM_001142424.1 | 701 | Missense Mutation | AAC,AGC | N,S 66 | NP_001135896.1 | |
NM_001142425.1 | 701 | Missense Mutation | AAC,AGC | N,S 66 | NP_001135897.1 | |
NM_001142426.1 | 701 | Missense Mutation | AAC,AGC | N,S 66 | NP_001135898.1 | |
NM_001142427.1 | 701 | Missense Mutation | AAC,AGC | N,S 66 | NP_001135899.1 | |
NM_001142428.1 | 701 | Missense Mutation | AAC,AGC | N,S 66 | NP_001135900.1 | |
NM_001142429.1 | 701 | Intron | NP_001135901.1 | |||
NM_001142430.1 | 701 | Missense Mutation | AAC,AGC | N,S 66 | NP_001135902.1 | |
NM_001142431.1 | 701 | Missense Mutation | AAC,AGC | N,S 66 | NP_001135903.1 | |
NM_001142432.1 | 701 | Missense Mutation | AAC,AGC | N,S 66 | NP_001135904.1 | |
NM_012286.2 | 701 | Missense Mutation | AAC,AGC | N,S 66 | NP_036418.1 |