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CGGGCTCCAGTGGTCCGGGTCTGTG[C/G]AGGGCTGGGGCGACAGGACCGGCTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 143023 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LMNTD2 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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LMNTD2 - lamin tail domain containing 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_173573.2 | 1113 | Missense Mutation | TCC,TGC | S,C 345 | NP_775844.2 | |
XM_011519965.2 | 1113 | Missense Mutation | TCC,TGC | S,C 418 | XP_011518267.2 | |
XM_011519967.2 | 1113 | Missense Mutation | TCC,TGC | S,C 418 | XP_011518269.2 | |
XM_017017476.1 | 1113 | Missense Mutation | TCC,TGC | S,C 418 | XP_016872965.1 | |
XM_017017477.1 | 1113 | Missense Mutation | TCC,TGC | S,C 413 | XP_016872966.1 | |
XM_017017478.1 | 1113 | Missense Mutation | TCC,TGC | S,C 350 | XP_016872967.1 | |
XM_017017479.1 | 1113 | Missense Mutation | TCC,TGC | S,C 418 | XP_016872968.1 |
LRRC56 - leucine rich repeat containing 56 | ||||||
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There are no transcripts associated with this gene. |
MIR210HG - MIR210 host gene | ||||||
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There are no transcripts associated with this gene. |
RASSF7 - Ras association domain family member 7 | ||||||
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There are no transcripts associated with this gene. |