Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CAGCAGTTCATTATTAGACCATTGG[C/T]CAATCTGTACTTATTAAAGCAATGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616443 | ||||||||||||||||||||
Literature Links: |
ZMYM5 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 |
ZMYM5 - zinc finger MYM-type containing 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001039649.2 | 1738 | Intron | NP_001034738.1 | |||
NM_001039650.2 | 1738 | Intron | NP_001034739.1 | |||
NM_001142684.1 | 1738 | Missense Mutation | ACC,GCC | T,A 372 | NP_001136156.1 | |
XM_005266593.3 | 1738 | Missense Mutation | ACC,GCC | T,A 372 | XP_005266650.1 | |
XM_005266594.2 | 1738 | Missense Mutation | ACC,GCC | T,A 372 | XP_005266651.1 | |
XM_006719894.2 | 1738 | Missense Mutation | ACC,GCC | T,A 372 | XP_006719957.1 | |
XM_011535309.1 | 1738 | Missense Mutation | ACC,GCC | T,A 399 | XP_011533611.1 | |
XM_011535310.1 | 1738 | Missense Mutation | ACC,GCC | T,A 217 | XP_011533612.1 | |
XM_017020849.1 | 1738 | Missense Mutation | ACC,GCC | T,A 190 | XP_016876338.1 | |
XM_017020850.1 | 1738 | Missense Mutation | ACC,GCC | T,A 190 | XP_016876339.1 | |
XM_017020851.1 | 1738 | Intron | XP_016876340.1 |