Product Details

SNP ID

rs1048604

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:169083707 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ACTGAATACAGTCTGTTATTTACTT[A/C]TCTCTTTTAACATAAGGTTGGGAAC

Phenotype

MIM: 165215

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

MECOM PubMed Links

Gene Details

Gene

MECOM

Gene Name

MDS1 and EVI1 complex locus

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001105077.3	4623	UTR 3			NP_001098547.3
NM_001105078.3	4623	UTR 3			NP_001098548.2
NM_001163999.1	4623	UTR 3			NP_001157471.1
NM_001164000.1	4623	UTR 3			NP_001157472.1
NM_001205194.1	4623	UTR 3			NP_001192123.1
NM_004991.3	4623	UTR 3			NP_004982.2
NM_005241.3	4623	UTR 3			NP_005232.2
XM_005247213.3	4623	UTR 3			XP_005247270.1
XM_005247214.3	4623	UTR 3			XP_005247271.1
XM_005247215.3	4623	UTR 3			XP_005247272.1
XM_005247219.2	4623	UTR 3			XP_005247276.1
XM_005247220.2	4623	UTR 3			XP_005247277.1
XM_005247221.2	4623	UTR 3			XP_005247278.1
XM_005247223.2	4623	UTR 3			XP_005247280.1
XM_005247224.3	4623	UTR 3			XP_005247281.1
XM_005247225.3	4623	UTR 3			XP_005247282.1
XM_005247226.3	4623	UTR 3			XP_005247283.1
XM_011512546.2	4623	UTR 3			XP_011510848.1
XM_017005874.1	4623	UTR 3			XP_016861363.1
XM_017005875.1	4623	Intron			XP_016861364.1
XM_017005876.1	4623	UTR 3			XP_016861365.1
XM_017005877.1	4623	UTR 3			XP_016861366.1
XM_017005878.1	4623	Intron			XP_016861367.1

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