Product Details

SNP ID

rs140121548

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:20012482 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAAATGTCTTGGGGATAAGTTTCTG[C/G]GGCAGCGTGATCCACACCATTAACT

Phenotype

Polymorphism

C/G, Transversion 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	1828	Missense Mutation	CCA,GCA	P647A	NP_001161937.1
NM_001168466.1	1828	Missense Mutation	CCA,GCA	P561A	NP_001161938.1
NM_001168467.1	1828	Missense Mutation	CCA,GCA	P554A	NP_001161939.1
NM_152780.3	1828	Missense Mutation	CCA,GCA	P606A	NP_689993.2
XM_005274478.2	1828	Missense Mutation	CCA,GCA	P631A	XP_005274535.1
XM_005274479.2	1828	Missense Mutation	CCA,GCA	P620A	XP_005274536.1
XM_005274480.3	1828	Missense Mutation	CCA,GCA	P598A	XP_005274537.1
XM_006724481.2	1828	Missense Mutation	CCA,GCA	P680A	XP_006724544.1
XM_006724482.2	1828	Missense Mutation	CCA,GCA	P639A	XP_006724545.1
XM_011545483.1	1828	Missense Mutation	CCA,GCA	P669A	XP_011543785.1
XM_011545484.1	1828	Missense Mutation	CCA,GCA	P636A	XP_011543786.1
XM_011545485.1	1828	Missense Mutation	CCA,GCA	P625A	XP_011543787.1
XM_011545486.2	1828	Intron			XP_011543788.1
XM_017029393.1	1828	Missense Mutation	CCA,GCA	P628A	XP_016884882.1
XM_017029394.1	1828	Missense Mutation	CCA,GCA	P595A	XP_016884883.1
XM_017029395.1	1828	Missense Mutation	CCA,GCA	P587A	XP_016884884.1
XM_017029396.1	1828	Missense Mutation	CCA,GCA	P584A	XP_016884885.1
XM_017029397.1	1828	Missense Mutation	CCA,GCA	P576A	XP_016884886.1
XM_017029398.1	1828	Intron			XP_016884887.1

Gene

MIR23C

Gene Name

microRNA 23c

There are no transcripts associated with this gene.

View Full Product Details