Product Details

SNP ID

rs201960499

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:20012470 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGCCCATTAGAGAAAATGTCTTGGG[A/G]ATAAGTTTCTGGGGCAGCGTGATCC

Phenotype

Polymorphism

A/G, 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	1840	Missense Mutation	CCC,TCC	P651S	NP_001161937.1
NM_001168466.1	1840	Missense Mutation	CCC,TCC	P565S	NP_001161938.1
NM_001168467.1	1840	Missense Mutation	CCC,TCC	P558S	NP_001161939.1
NM_152780.3	1840	Missense Mutation	CCC,TCC	P610S	NP_689993.2
XM_005274478.2	1840	Missense Mutation	CCC,TCC	P635S	XP_005274535.1
XM_005274479.2	1840	Missense Mutation	CCC,TCC	P624S	XP_005274536.1
XM_005274480.3	1840	Missense Mutation	CCC,TCC	P602S	XP_005274537.1
XM_006724481.2	1840	Missense Mutation	CCC,TCC	P684S	XP_006724544.1
XM_006724482.2	1840	Missense Mutation	CCC,TCC	P643S	XP_006724545.1
XM_011545483.1	1840	Missense Mutation	CCC,TCC	P673S	XP_011543785.1
XM_011545484.1	1840	Missense Mutation	CCC,TCC	P640S	XP_011543786.1
XM_011545485.1	1840	Missense Mutation	CCC,TCC	P629S	XP_011543787.1
XM_011545486.2	1840	Intron			XP_011543788.1
XM_017029393.1	1840	Missense Mutation	CCC,TCC	P632S	XP_016884882.1
XM_017029394.1	1840	Missense Mutation	CCC,TCC	P599S	XP_016884883.1
XM_017029395.1	1840	Missense Mutation	CCC,TCC	P591S	XP_016884884.1
XM_017029396.1	1840	Missense Mutation	CCC,TCC	P588S	XP_016884885.1
XM_017029397.1	1840	Missense Mutation	CCC,TCC	P580S	XP_016884886.1
XM_017029398.1	1840	Intron			XP_016884887.1

Gene

MIR23C

Gene Name

microRNA 23c

There are no transcripts associated with this gene.

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