Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTGCTCCGCGGAGATGTGTGTGATA[C/T]GCCGGTTCTCGGTCTCGGGGAGCAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605678 | ||||||||||||||||||||
Literature Links: |
MLXIPL 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 |
MLXIPL - MLX interacting protein like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_032951.2 | 2000 | Missense Mutation | CAT,CGT | H,R 651 | NP_116569.1 | |
NM_032952.2 | 2000 | Missense Mutation | CAT,CGT | H,R 651 | NP_116570.1 | |
NM_032953.2 | 2000 | Missense Mutation | CAT,CGT | H,R 649 | NP_116571.1 | |
NM_032954.2 | 2000 | Missense Mutation | CAT,CGT | H,R 649 | NP_116572.1 | |
XM_011516277.1 | 2000 | Missense Mutation | CAT,CGT | H,R 716 | XP_011514579.1 | |
XM_011516278.1 | 2000 | Missense Mutation | CAT,CGT | H,R 715 | XP_011514580.1 | |
XM_011516279.1 | 2000 | Missense Mutation | CAT,CGT | H,R 716 | XP_011514581.1 | |
XM_011516281.2 | 2000 | Missense Mutation | CAT,CGT | H,R 375 | XP_011514583.1 | |
XM_017012263.1 | 2000 | Missense Mutation | CAT,CGT | H,R 348 | XP_016867752.1 |