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SNP ID

hCV27460141

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:87116841 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GATTGATCTTGGCCTGGATTTTATG[C/T]GTCAGTGTGACAGAGAGGGTAAGGA

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FAM35A PubMed Links

Gene Details

Gene

FAM35A

Gene Name

family with sequence similarity 35 member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_019054.2		Intron			NP_061927.2

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