Product Details

SNP ID

rs496226

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.18:320398 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTGTTTAGATATCTGTGTTTTTCCC[C/G]CTCAACTGACCCAGCTGTGAGTTCC

Phenotype

MIM: 607621

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

COLEC12 PubMed Links

Gene Details

Gene

COLEC12

Gene Name

collectin subfamily member 12

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_130386.2		Intron			NP_569057.1
XM_011525741.2		Intron			XP_011524043.1

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