Product Details

SNP ID

hCV27974219

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:37391423 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTGCACCTTGGGCATCTCTTTTAAG[A/G]AGAAAGGAGAAGGAGGAGAAAGGGG

Phenotype

MIM: 611429

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

C3orf35 PubMed Links

Gene Details

Gene

C3orf35

Gene Name

chromosome 3 open reading frame 35

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001302831.1		Intron			NP_001289760.1
NM_001302832.1		Intron			NP_001289761.1
NM_178339.2		Intron			NP_848029.2
NM_178342.2		Intron			NP_848032.1
NM_178344.2		Intron			NP_848034.2

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