Product Details

SNP ID

rs521990

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.20:841832 on Build GRCh38

Set Membership

Validated

Context Sequence [VIC/FAM]

CTGGCTTCACCTGGCGGGAGCCGCT[C/G]CACCTCCGTTTGCCCACCCGTGACG

Phenotype

MIM: 611393

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

FAM110A PubMed Links

Gene Details

Gene

FAM110A

Gene Name

family with sequence similarity 110 member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001042353.2	481	Intron			NP_001035812.1
NM_001289145.1	481	Intron			NP_001276074.1
NM_001289146.1	481	Intron			NP_001276075.1
NM_001289147.1	481	Intron			NP_001276076.1
NM_031424.5	481	Intron			NP_113612.1
NM_207121.4	481	Intron			NP_997004.1
XM_011529381.2	481	UTR 5			XP_011527683.1

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