Product Details

SNP ID
rs4596614
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.8:91216289 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CTTTGCATTCCTGCTTGCAATAAGA[A/G]CCAACCTAAACTCTGCCCATGCGAT
Phenotype
MIM: 608479
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
LRRC69 PubMed Links

Gene Details

Gene
LRRC69
Gene Name
leucine rich repeat containing 69
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001129890.1 Intron NP_001123362.1
Gene
SLC26A7
Gene Name
solute carrier family 26 member 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001282356.1 Intron NP_001269285.1
NM_001282357.1 Intron NP_001269286.1
NM_052832.3 Intron NP_439897.1
NM_134266.1 Intron NP_599028.1

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