Product Details

SNP ID
rs142539088
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:59148952 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATGAAAATCGAGCACTATTTTTCTC[C/T]GGTATGTCTGTAAATTCTACTTATG
Phenotype
MIM: 615292
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
FAM111A PubMed Links

Gene Details

Gene
FAM111A
Gene Name
family with sequence similarity 111 member A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001142519.2 265 Missense Mutation CCG,CTG P27L NP_001135991.1
NM_001142520.2 265 Missense Mutation CCG,CTG P27L NP_001135992.1
NM_001142521.2 265 Missense Mutation CCG,CTG P27L NP_001135993.1
NM_001312909.1 265 Missense Mutation CCG,CTG P27L NP_001299838.1
NM_001312910.1 265 Missense Mutation CCG,CTG P27L NP_001299839.1
NM_001312911.1 265 Missense Mutation CCG,CTG P27L NP_001299840.1
NM_022074.3 265 Missense Mutation CCG,CTG P27L NP_071357.2
NM_198847.2 265 Missense Mutation CCG,CTG P27L NP_942144.1
Gene
LOC101927204
Gene Name
uncharacterized LOC101927204
There are no transcripts associated with this gene.

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