Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GAGTGCCGGGATGTGCTGCTAGAGT[C/T]GGTGGAACACCACCTCACGCCCAAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
3 submissions
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Phenotype: |
MIM: 608095 MIM: 612112 | ||||||||||||||||||||
Literature Links: |
LYSMD1 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 |
LYSMD1 - LysM domain containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001136543.1 | 515 | Intron | NP_001130015.1 | |||
NM_212551.4 | 515 | Intron | NP_997716.1 |
SCNM1 - sodium channel modifier 1 | ||||||
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There are no transcripts associated with this gene. |
TNFAIP8L2 - TNF alpha induced protein 8 like 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_024575.4 | 515 | Missense Mutation | TCG,TTG | S,L 130 | NP_078851.2 |
TNFAIP8L2-SCNM1 - TNFAIP8L2-SCNM1 readthrough | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001204848.1 | 515 | Intron | NP_001191777.1 |