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Search Thermo Fisher Scientific
GAAGGAGACGATTGGAGTCAACTCA[A/G]TGTGCTCAAAGTAAGCGTGAGCGGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
16 submissions
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Phenotype: |
MIM: 608095 MIM: 605834 MIM: 612112 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LYSMD1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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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 | 172 | Intron | NP_001130015.1 | |||
NM_212551.4 | 172 | Intron | NP_997716.1 |
SCNM1 - sodium channel modifier 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001204856.1 | 172 | UTR 5 | NP_001191785.1 | |||
NM_024041.3 | 172 | Missense Mutation | AAT,AGT | N,S 14 | NP_076946.1 |
TMOD4 - tropomodulin 4 | ||||||
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There are no transcripts associated with this gene. |
TNFAIP8L2 - TNF alpha induced protein 8 like 2 | ||||||
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There are no transcripts associated with this gene. |
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 | 172 | Intron | NP_001191777.1 |