Product Details

SNP ID

rs146751566

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:54885289 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAATCGAGTCCTGTGATTCCCTTGG[A/G]TGGATCTGTGAAAATCCAGTGCCAG

Phenotype

MIM: 147045

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

FCAR PubMed Links

Gene Details

Gene

FCAR

Gene Name

Fc fragment of IgA receptor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002000.3	286	Missense Mutation	GAT,GGT	D42G	NP_001991.1
NM_133269.3	286	Missense Mutation	GAT,GGT	D42G	NP_579803.1
NM_133271.3	286	Missense Mutation	GAT,GGT	D42G	NP_579805.1
NM_133272.3	286	Missense Mutation	GAT,GGT	D30G	NP_579806.1
NM_133273.3	286	Missense Mutation	GAT,GGT	D30G	NP_579807.1
NM_133274.3	286	Missense Mutation	GAT,GGT	D30G	NP_579808.1
NM_133277.3	286	Intron			NP_579811.1
NM_133278.3	286	Missense Mutation	GAT,GGT	D30G	NP_579812.1
XM_011526625.2	286	Missense Mutation	GAT,GGT	D15G	XP_011524927.1
XM_017026473.1	286	Missense Mutation	GAT,GGT	D15G	XP_016881962.1
XM_017026474.1	286	Missense Mutation	GAT,GGT	D15G	XP_016881963.1

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