Product Details

SNP ID

rs879072

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:3646625 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AAGCAGGTGCCGCTGCCTCGCCTGC[C/T]GGAAGGGAGCCCGTCAGAGCGACCA

Phenotype

MIM: 612396 MIM: 612502

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

ALLC PubMed Links

Gene Details

Gene

ALLC

Gene Name

allantoicase

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_018436.3	1098	Intron			NP_060906.3
XM_011510369.2	1098	Intron			XP_011508671.1
XM_011510370.2	1098	Intron			XP_011508672.1
XM_017004495.1	1098	Missense Mutation	CCG,CTG	P21L	XP_016859984.1
XM_017004496.1	1098	Intron			XP_016859985.1
XM_017004497.1	1098	Intron			XP_016859986.1
XM_017004498.1	1098	Intron			XP_016859987.1

Gene

COLEC11

Gene Name

collectin subfamily member 11

There are no transcripts associated with this gene.

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