Product Details

SNP ID

rs111803813

Assay Type

Functionally tested

NCBI dbSNP Submissions

1

Location

Chr.1:31364132 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAGAGGGCAAGGCACACATCAAAAG[A/G]CAGCAAGGCAGCAAAGAAGAAGAAA

Phenotype

MIM: 134651

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

FABP3 PubMed Links

Gene Details

Gene

FABP3

Gene Name

fatty acid binding protein 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001320996.1	958	Intron			NP_001307925.1
NM_004102.4	958	Intron			NP_004093.1
XM_011541007.2	958	Intron			XP_011539309.1

Gene

ZCCHC17

Gene Name

zinc finger CCHC-type containing 17

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001282566.1	958	Missense Mutation	GAC,GGC	D244G	NP_001269495.1
NM_001282567.1	958	Missense Mutation	GAC,GGC	D224G	NP_001269496.1
NM_001282568.1	958	Missense Mutation	GAC,GGC	D222G	NP_001269497.1
NM_001282569.1	958	Missense Mutation	GAC,GGC	D214G	NP_001269498.1
NM_001282570.1	958	Missense Mutation	GAC,GGC	D198G	NP_001269499.1
NM_001282571.1	958	Missense Mutation	GAC,GGC	D160G	NP_001269500.1
NM_001282572.1	958	Missense Mutation	ACA,GCA	T140A	NP_001269501.1
NM_001282573.1	958	Missense Mutation	ACA,GCA	T132A	NP_001269502.1
NM_001282574.1	958	UTR 3			NP_001269503.1
NM_016505.3	958	Missense Mutation	GAC,GGC	D222G	NP_057589.2
XM_006710681.3	958	Missense Mutation	GAC,GGC	D214G	XP_006710744.1
XM_011541567.2	958	Missense Mutation	GAC,GGC	D222G	XP_011539869.1

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