Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGTTCAGAACTTGCCCTGCTTCAGC[C/T]GGTCAATGTGGTAGGAGAGCTTGAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
5 submissions
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Phenotype: |
MIM: 616396 | ||||||||||||||||||||
Literature Links: |
SCMH1 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
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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 |
SCMH1 - sex comb on midleg homolog 1 (Drosophila) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001031694.2 | 2193 | Missense Mutation | CAG,CGG | Q,R 654 | NP_001026864.1 | |
NM_001172218.1 | 2193 | Missense Mutation | CAG,CGG | Q,R 571 | NP_001165689.1 | |
NM_001172219.1 | 2193 | Missense Mutation | CAG,CGG | Q,R 642 | NP_001165690.1 | |
NM_001172220.1 | 2193 | Missense Mutation | CAG,CGG | Q,R 571 | NP_001165691.1 | |
NM_001172221.1 | 2193 | Missense Mutation | CAG,CGG | Q,R 593 | NP_001165692.1 | |
NM_001172222.2 | 2193 | Missense Mutation | CAG,CGG | Q,R 474 | NP_001165693.1 | |
NM_012236.3 | 2193 | Missense Mutation | CAG,CGG | Q,R 585 | NP_036368.1 | |
XM_006710462.2 | 2193 | Missense Mutation | CAG,CGG | Q,R 664 | XP_006710525.1 | |
XM_006710464.1 | 2193 | Missense Mutation | CAG,CGG | Q,R 593 | XP_006710527.1 | |
XM_011541032.2 | 2193 | Missense Mutation | CAG,CGG | Q,R 664 | XP_011539334.1 | |
XM_011541033.2 | 2193 | Missense Mutation | CAG,CGG | Q,R 654 | XP_011539335.1 | |
XM_011541034.1 | 2193 | UTR 3 | XP_011539336.1 | |||
XM_011541035.2 | 2193 | Missense Mutation | CAG,CGG | Q,R 607 | XP_011539337.1 | |
XM_011541036.2 | 2193 | Missense Mutation | CAG,CGG | Q,R 593 | XP_011539338.1 | |
XM_011541039.1 | 2193 | Missense Mutation | CAG,CGG | Q,R 544 | XP_011539341.1 | |
XM_011541040.2 | 2193 | Intron | XP_011539342.1 | |||
XM_011541043.2 | 2193 | Missense Mutation | CAG,CGG | Q,R 486 | XP_011539345.1 | |
XM_011541044.1 | 2193 | Missense Mutation | CAG,CGG | Q,R 486 | XP_011539346.1 | |
XM_011541045.2 | 2193 | Missense Mutation | CAG,CGG | Q,R 563 | XP_011539347.2 | |
XM_017000698.1 | 2193 | Missense Mutation | CAG,CGG | Q,R 612 | XP_016856187.1 | |
XM_017000699.1 | 2193 | Missense Mutation | CAG,CGG | Q,R 593 | XP_016856188.1 | |
XM_017000700.1 | 2193 | UTR 3 | XP_016856189.1 | |||
XM_017000701.1 | 2193 | Missense Mutation | CAG,CGG | Q,R 553 | XP_016856190.1 | |
XM_017000702.1 | 2193 | Missense Mutation | CAG,CGG | Q,R 541 | XP_016856191.1 | |
XM_017000703.1 | 2193 | Missense Mutation | CAG,CGG | Q,R 541 | XP_016856192.1 | |
XM_017000704.1 | 2193 | Missense Mutation | CAG,CGG | Q,R 531 | XP_016856193.1 | |
XM_017000705.1 | 2193 | Missense Mutation | CAG,CGG | Q,R 496 | XP_016856194.1 | |
XM_017000706.1 | 2193 | Missense Mutation | CAG,CGG | Q,R 482 | XP_016856195.1 | |
XM_017000707.1 | 2193 | Missense Mutation | CAG,CGG | Q,R 474 | XP_016856196.1 | |
XM_017000708.1 | 2193 | Missense Mutation | CAG,CGG | Q,R 473 | XP_016856197.1 | |
XM_017000709.1 | 2193 | Missense Mutation | CAG,CGG | Q,R 464 | XP_016856198.1 | |
XM_017000710.1 | 2193 | Missense Mutation | CAG,CGG | Q,R 460 | XP_016856199.1 | |
XM_017000711.1 | 2193 | Missense Mutation | CAG,CGG | Q,R 451 | XP_016856200.1 | |
XM_017000712.1 | 2193 | Missense Mutation | CAG,CGG | Q,R 451 | XP_016856201.1 | |
XM_017000713.1 | 2193 | Missense Mutation | CAG,CGG | Q,R 443 | XP_016856202.1 |
SLFNL1 - schlafen like 1 | ||||||
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There are no transcripts associated with this gene. |
SLFNL1-AS1 - SLFNL1 antisense RNA 1 | ||||||
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There are no transcripts associated with this gene. |