Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCATCGTAGTCTATCTGGAAGTGGC[A/G]GGACTCCCTGATTGACTGGTCATCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600922 | ||||||||||||||||||||
Literature Links: |
MYLK 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 |
MYLK - myosin light chain kinase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001321309.1 | 2156 | Missense Mutation | CGC,TGC | R,C 1677 | NP_001308238.1 | |
NM_053025.3 | 2156 | Missense Mutation | CGC,TGC | R,C 1853 | NP_444253.3 | |
NM_053026.3 | 2156 | Missense Mutation | CGC,TGC | R,C 1784 | NP_444254.3 | |
NM_053027.3 | 2156 | Missense Mutation | CGC,TGC | R,C 1802 | NP_444255.3 | |
NM_053028.3 | 2156 | Missense Mutation | CGC,TGC | R,C 1733 | NP_444256.3 | |
XM_011512860.2 | 2156 | Missense Mutation | CGC,TGC | R,C 1852 | XP_011511162.1 | |
XM_011512861.2 | 2156 | Missense Mutation | CGC,TGC | R,C 1785 | XP_011511163.1 | |
XM_017006469.1 | 2156 | Missense Mutation | CGC,TGC | R,C 930 | XP_016861958.1 | |
XM_017006470.1 | 2156 | Missense Mutation | CGC,TGC | R,C 652 | XP_016861959.1 | |
XM_017006471.1 | 2156 | Missense Mutation | CGC,TGC | R,C 653 | XP_016861960.1 | |
XM_017006472.1 | 2156 | Missense Mutation | CGC,TGC | R,C 93 | XP_016861961.1 | |
XM_017006473.1 | 2156 | Missense Mutation | CGC,TGC | R,C 92 | XP_016861962.1 |
MYLK-AS1 - MYLK antisense RNA 1 | ||||||
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There are no transcripts associated with this gene. |