Product Details

SNP ID
rs200079468
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.11:562256 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGGAGGCCCTCCTCAGACAGCTGTC[C/T]ACCCCCGGAACGCTGCCTAATTCGT
Phenotype
MIM: 612982 MIM: 143023
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
LMNTD2 PubMed Links

Gene Details

Gene
LMNTD2
Gene Name
lamin tail domain containing 2
There are no transcripts associated with this gene.

Gene
LRRC56
Gene Name
leucine rich repeat containing 56
There are no transcripts associated with this gene.

Gene
MIR210
Gene Name
microRNA 210
There are no transcripts associated with this gene.

Gene
MIR210HG
Gene Name
MIR210 host gene
There are no transcripts associated with this gene.

Gene
RASSF7
Gene Name
Ras association domain family member 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001143993.1 740 Missense Mutation CCA,CTA P101L NP_001137465.1
NM_001143994.1 740 Missense Mutation CCA,CTA P101L NP_001137466.1
NM_003475.3 740 Missense Mutation CCA,CTA P101L NP_003466.1
XM_005253149.3 740 Missense Mutation CCA,CTA P149L XP_005253206.2
XM_005253150.1 740 Missense Mutation CCA,CTA P101L XP_005253207.1
XM_006718338.2 740 Missense Mutation CCA,CTA P101L XP_006718401.1
XM_011520389.1 740 Missense Mutation CCA,CTA P101L XP_011518691.1
XM_017018360.1 740 Missense Mutation CCA,CTA P149L XP_016873849.1
XM_017018361.1 740 Missense Mutation CCA,CTA P101L XP_016873850.1
XM_017018362.1 740 Missense Mutation CCA,CTA P101L XP_016873851.1

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