Product Details

SNP ID
rs151110994
Assay Type
Functionally tested
NCBI dbSNP Submissions
16
Location
Chr.1:70145857 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTATAGCAGCTGTTCCTTTCATTAA[C/T]ATGGCTGCTCGAGGAACTCGGAATG
Phenotype
MIM: 614453
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
LRRC40 PubMed Links

Gene Details

Gene
LRRC40
Gene Name
leucine rich repeat containing 40
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_017768.4 1632 Missense Mutation ATA,ATG I584M NP_060238.3
XM_005271013.1 1632 Missense Mutation ATA,ATG I366M XP_005271070.1
XM_011541763.1 1632 Missense Mutation ATA,ATG I366M XP_011540065.1
XM_017001695.1 1632 Missense Mutation ATA,ATG I343M XP_016857184.1
XM_017001696.1 1632 Missense Mutation ATA,ATG I343M XP_016857185.1
Gene
LRRC7
Gene Name
leucine rich repeat containing 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_020794.2 1632 Intron NP_065845.1
XM_017001885.1 1632 Intron XP_016857374.1
XM_017001886.1 1632 Intron XP_016857375.1
XM_017001887.1 1632 Intron XP_016857376.1
XM_017001888.1 1632 Intron XP_016857377.1
XM_017001889.1 1632 Intron XP_016857378.1
XM_017001890.1 1632 Intron XP_016857379.1
XM_017001891.1 1632 Intron XP_016857380.1
XM_017001892.1 1632 Intron XP_016857381.1
XM_017001893.1 1632 Intron XP_016857382.1
XM_017001894.1 1632 Intron XP_016857383.1
XM_017001895.1 1632 Intron XP_016857384.1

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