Product Details

SNP ID

rs147455037

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.22:38113560 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGCCAGCTCCCAGGGGTTGCTGGGA[C/T]GGAAGACATCCACACAGGTCACAGG

Phenotype

MIM: 603604

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

BAIAP2L2 PubMed Links

Gene Details

Gene

BAIAP2L2

Gene Name

BAI1 associated protein 2 like 2

There are no transcripts associated with this gene.

Gene

PLA2G6

Gene Name

phospholipase A2 group VI

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001004426.1	2314	Missense Mutation	CAT,CGT	H656R	NP_001004426.1
NM_001199562.1	2314	Missense Mutation	CAT,CGT	H656R	NP_001186491.1
NM_003560.2	2314	Missense Mutation	CAT,CGT	H710R	NP_003551.2
XM_005261764.2	2314	Missense Mutation	CAT,CGT	H710R	XP_005261821.1
XM_005261765.1	2314	Missense Mutation	CAT,CGT	H710R	XP_005261822.1
XM_005261766.1	2314	Missense Mutation	CAT,CGT	H710R	XP_005261823.1
XM_006724332.3	2314	Missense Mutation	CAT,CGT	H710R	XP_006724395.1
XM_011530422.1	2314	Missense Mutation	CAT,CGT	H675R	XP_011528724.1
XM_011530423.1	2314	Missense Mutation	CAT,CGT	H532R	XP_011528725.1
XM_011530424.1	2314	Missense Mutation	CAT,CGT	H532R	XP_011528726.1
XM_011530425.1	2314	Missense Mutation	CAT,CGT	H532R	XP_011528727.1
XM_011530426.2	2314	Intron			XP_011528728.1
XM_017028981.1	2314	Missense Mutation	CAT,CGT	H656R	XP_016884470.1
XM_017028982.1	2314	Missense Mutation	CAT,CGT	H656R	XP_016884471.1
XM_017028983.1	2314	Missense Mutation	CAT,CGT	H478R	XP_016884472.1
XM_017028984.1	2314	Missense Mutation	CAT,CGT	H478R	XP_016884473.1
XM_017028985.1	2314	Missense Mutation	CAT,CGT	H484R	XP_016884474.1
XM_017028986.1	2314	Intron			XP_016884475.1
XM_017028987.1	2314	Intron			XP_016884476.1
XM_017028988.1	2314	Intron			XP_016884477.1

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