Product Details

SNP ID

rs2075278

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.22:21028993 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCCACAACAGAAGGGGCTCTCGGCT[C/T]GTCTGGCCTCTCTGGCCTCCCAAGC

Phenotype

MIM: 608077 MIM: 603752

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MIR649 PubMed Links

Gene Details

Gene

MIR649

Gene Name

microRNA 649

There are no transcripts associated with this gene.

Gene

P2RX6

Gene Name

purinergic receptor P2X 6

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001159554.1	2038	Intron			NP_001153026.1
NM_005446.3	2038	Intron			NP_005437.2
XM_005261819.3	2038	Intron			XP_005261876.1
XM_011530498.2	2038	Intron			XP_011528800.1
XM_011530499.2	2038	Intron			XP_011528801.1
XM_011530500.2	2038	Intron			XP_011528802.1
XM_011530501.2	2038	Intron			XP_011528803.1
XM_011530502.2	2038	Intron			XP_011528804.1
XM_017029066.1	2038	Intron			XP_016884555.1
XM_017029067.1	2038	Intron			XP_016884556.1
XM_017029068.1	2038	Intron			XP_016884557.1
XM_017029069.1	2038	Intron			XP_016884558.1
XM_017029070.1	2038	Intron			XP_016884559.1
XM_017029071.1	2038	Intron			XP_016884560.1
XM_017029072.1	2038	Intron			XP_016884561.1
XM_017029073.1	2038	Intron			XP_016884562.1
XM_017029074.1	2038	Intron			XP_016884563.1
XM_017029075.1	2038	Intron			XP_016884564.1
XM_017029076.1	2038	Intron			XP_016884565.1

Gene

SLC7A4

Gene Name

solute carrier family 7 member 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_004173.2	2038	UTR 3			NP_004164.2

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