Product Details

SNP ID
rs200149562
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:43335110 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGAATCATTTTTTTCCTGCTAAAAT[G/T]ATAGAGGCAGAAGAGCAACAGCCTT
Phenotype
MIM: 611246
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
ADAL PubMed Links

Gene Details

Gene
ADAL
Gene Name
adenosine deaminase like
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001012969.3 608 Missense Mutation ATG,ATT M1I NP_001012987.1
NM_001159280.2 608 Missense Mutation ATG,ATT M1I NP_001152752.1
NM_001324364.1 608 Missense Mutation ATG,ATT M1I NP_001311293.1
NM_001324365.1 608 Missense Mutation ATG,ATT M1I NP_001311294.1
NM_001324366.1 608 Missense Mutation ATG,ATT M1I NP_001311295.1
NM_001324367.1 608 Missense Mutation ATG,ATT M1I NP_001311296.1
NM_001324368.1 608 Missense Mutation ATG,ATT M1I NP_001311297.1
XM_011521291.2 608 Missense Mutation ATG,ATT M1I XP_011519593.1
XM_017021964.1 608 Missense Mutation ATG,ATT M1I XP_016877453.1
XM_017021965.1 608 Missense Mutation ATG,ATT M1I XP_016877454.1
XM_017021966.1 608 Missense Mutation ATG,ATT M1I XP_016877455.1
XM_017021967.1 608 Intron XP_016877456.1
XM_017021968.1 608 Missense Mutation ATG,ATT M1I XP_016877457.1
XM_017021969.1 608 Missense Mutation ATG,ATT M1I XP_016877458.1
Gene
LCMT2
Gene Name
leucine carboxyl methyltransferase 2
There are no transcripts associated with this gene.

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