Product Details

SNP ID

rs11691572

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:264985 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GGAAGATGGCGGAACAGGCTACCAA[G/T]TCCGTGCTGTTTGTGTGTCTGGGTA

Phenotype

MIM: 171500

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

ACP1 PubMed Links

Gene Details

Gene

ACP1

Gene Name

acid phosphatase 1, soluble

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001040649.2	117	Silent Mutation	AAG,AAT	K7N	NP_001035739.1
NM_004300.3	117	Intron			NP_004291.1
NM_007099.3	117	Intron			NP_009030.1

Gene

SH3YL1

Gene Name

SH3 and SYLF domain containing 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001159597.2	117	Intron			NP_001153069.1
NM_001282682.1	117	Intron			NP_001269611.1
NM_001282687.1	117	Intron			NP_001269616.1
NM_015677.3	117	Intron			NP_056492.2

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