Product Details

SNP ID

rs202062315

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:20015302 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAGACGCATCTGTTCAGCTACCTCC[C/T]GGGCCTTTGTTTCTGCTGCTTCTTT

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MAP7D2 PubMed Links

Gene Details

Gene

MAP7D2

Gene Name

MAP7 domain containing 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001168465.1	1559	Missense Mutation	CAG,CGG	Q557R	NP_001161937.1
NM_001168466.1	1559	Missense Mutation	CAG,CGG	Q471R	NP_001161938.1
NM_001168467.1	1559	Missense Mutation	CAG,CGG	Q464R	NP_001161939.1
NM_152780.3	1559	Missense Mutation	CAG,CGG	Q516R	NP_689993.2
XM_005274478.2	1559	Missense Mutation	CAG,CGG	Q541R	XP_005274535.1
XM_005274479.2	1559	Missense Mutation	CAG,CGG	Q530R	XP_005274536.1
XM_005274480.3	1559	Missense Mutation	CAG,CGG	Q508R	XP_005274537.1
XM_006724481.2	1559	Missense Mutation	CAG,CGG	Q590R	XP_006724544.1
XM_006724482.2	1559	Missense Mutation	CAG,CGG	Q549R	XP_006724545.1
XM_011545483.1	1559	Missense Mutation	CAG,CGG	Q579R	XP_011543785.1
XM_011545484.1	1559	Missense Mutation	CAG,CGG	Q546R	XP_011543786.1
XM_011545485.1	1559	Missense Mutation	CAG,CGG	Q535R	XP_011543787.1
XM_011545486.2	1559	Intron			XP_011543788.1
XM_017029393.1	1559	Missense Mutation	CAG,CGG	Q538R	XP_016884882.1
XM_017029394.1	1559	Missense Mutation	CAG,CGG	Q505R	XP_016884883.1
XM_017029395.1	1559	Missense Mutation	CAG,CGG	Q497R	XP_016884884.1
XM_017029396.1	1559	Missense Mutation	CAG,CGG	Q494R	XP_016884885.1
XM_017029397.1	1559	Missense Mutation	CAG,CGG	Q486R	XP_016884886.1
XM_017029398.1	1559	Intron			XP_016884887.1

Gene

MIR23C

Gene Name

microRNA 23c

There are no transcripts associated with this gene.

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