Product Details

SNP ID
rs201784529
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:115093960 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGTGCGAGAGGACCGGCTCCTGCTT[C/T]TCGGGCCGCTGTGTCAACTCCACCT
Phenotype
MIM: 612869
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
ATRNL1 PubMed Links

Gene Details

Gene
ATRNL1
Gene Name
attractin like 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001276282.3 591 Silent Mutation TTC,TTT F70F NP_001263211.1
NM_207303.4 591 Silent Mutation TTC,TTT F70F NP_997186.1
XM_011539587.1 591 Silent Mutation TTC,TTT F70F XP_011537889.1
XM_011539588.2 591 Intron XP_011537890.1
XM_011539589.2 591 Silent Mutation TTC,TTT F70F XP_011537891.1
XM_011539590.2 591 Intron XP_011537892.1
XM_011539591.2 591 Intron XP_011537893.1
XM_017016035.1 591 Silent Mutation TTC,TTT F70F XP_016871524.1
XM_017016036.1 591 Silent Mutation TTC,TTT F70F XP_016871525.1
XM_017016037.1 591 Intron XP_016871526.1
XM_017016038.1 591 Intron XP_016871527.1
XM_017016039.1 591 Intron XP_016871528.1
XM_017016040.1 591 Intron XP_016871529.1

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