Product Details

SNP ID
rs77681433
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:73411024 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGGGTTAGGGAGAAAAGACTAAGAC[A/G]TTGGGGTCTCACCTTGACCAACCAA
Phenotype
MIM: 616316
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
FAM168A PubMed Links

Gene Details

Gene
FAM168A
Gene Name
family with sequence similarity 168 member A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001286050.1 Intron NP_001272979.1
NM_001286051.1 Intron NP_001272980.1
NM_015159.2 Intron NP_055974.1
XM_017017415.1 Intron XP_016872904.1
XM_017017416.1 Intron XP_016872905.1

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