Product Details

SNP ID
rs139441878
Assay Type
Functionally tested
NCBI dbSNP Submissions
10
Location
Chr.1:156096374 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTTTCCCATCTATAAAGTGAAGCTA[A/G]TAGTAGCAATTACCTCATGGGATTG
Phenotype
MIM: 150330
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
LMNA PubMed Links

Gene Details

Gene
LMNA
Gene Name
lamin A/C
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001257374.2 Intron NP_001244303.1
NM_001282624.1 Intron NP_001269553.1
NM_001282625.1 Intron NP_001269554.1
NM_001282626.1 Intron NP_001269555.1
NM_005572.3 Intron NP_005563.1
NM_170707.3 Intron NP_733821.1
NM_170708.3 Intron NP_733822.1
XM_011509533.1 Intron XP_011507835.1
XM_011509534.1 Intron XP_011507836.1

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