Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ACCTGGACGAGCCCATCAAAATCGG[C/T]CGCTCAGTGGCCCGCTGTCGACCAG
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 602701 | |||||||||||||||||||||||
Literature Links: |
SLMAP PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
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 |
SLMAP - sarcolemma associated protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001304420.2 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | NP_001291349.1 | |
NM_001304421.2 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | NP_001291350.1 | |
NM_001304422.2 | 1319 | Intron | NP_001291351.1 | |||
NM_001304423.2 | 1319 | Intron | NP_001291352.1 | |||
NM_001311178.1 | 1319 | Intron | NP_001298107.1 | |||
NM_001311179.1 | 1319 | Intron | NP_001298108.1 | |||
NM_007159.4 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | NP_009090.2 | |
XM_005265456.3 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_005265513.1 | |
XM_005265457.3 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_005265514.1 | |
XM_005265458.3 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_005265515.1 | |
XM_005265459.3 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_005265516.1 | |
XM_005265460.3 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_005265517.1 | |
XM_005265461.3 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_005265518.1 | |
XM_005265462.3 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_005265519.1 | |
XM_005265464.3 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_005265521.1 | |
XM_005265465.3 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_005265522.1 | |
XM_005265466.3 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_005265523.1 | |
XM_005265467.3 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_005265524.1 | |
XM_005265468.3 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_005265525.1 | |
XM_005265470.3 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_005265527.1 | |
XM_005265471.3 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_005265528.1 | |
XM_005265472.3 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_005265529.1 | |
XM_006713326.2 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_006713389.1 | |
XM_011534103.1 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_011532405.1 | |
XM_011534104.1 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_011532406.1 | |
XM_011534105.1 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_011532407.1 | |
XM_011534106.1 | 1319 | Intron | XP_011532408.1 | |||
XM_017007146.1 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_016862635.1 | |
XM_017007147.1 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_016862636.1 | |
XM_017007148.1 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_016862637.1 | |
XM_017007149.1 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_016862638.1 | |
XM_017007150.1 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_016862639.1 | |
XM_017007151.1 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_016862640.1 | |
XM_017007152.1 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_016862641.1 | |
XM_017007153.1 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_016862642.1 | |
XM_017007154.1 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_016862643.1 | |
XM_017007155.1 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_016862644.1 | |
XM_017007156.1 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_016862645.1 | |
XM_017007157.1 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_016862646.1 | |
XM_017007158.1 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_016862647.1 | |
XM_017007159.1 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_016862648.1 | |
XM_017007160.1 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_016862649.1 | |
XM_017007161.1 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_016862650.1 | |
XM_017007162.1 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_016862651.1 | |
XM_017007163.1 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_016862652.1 | |
XM_017007164.1 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_016862653.1 | |
XM_017007165.1 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_016862654.1 | |
XM_017007166.1 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_016862655.1 | |
XM_017007167.1 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_016862656.1 | |
XM_017007168.1 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_016862657.1 | |
XM_017007169.1 | 1319 | Silent Mutation | GGC,GGT | G,G 31 | XP_016862658.1 | |
XM_017007170.1 | 1319 | Intron | XP_016862659.1 |