Product Details

SNP ID
rs1121878
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:69748175 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TTTAATTTGACATCTTTAAAAAAAT[A/C]TTCAAAGCATTTGGATTTTAGTAGC
Phenotype
MIM: 156845
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
MITF PubMed Links

Gene Details

Gene
MITF
Gene Name
melanogenesis associated transcription factor
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000248.3 Intron NP_000239.1
NM_001184967.1 Intron NP_001171896.1
NM_001184968.1 Intron NP_001171897.1
NM_006722.2 Intron NP_006713.1
NM_198158.2 Intron NP_937801.1
NM_198159.2 Intron NP_937802.1
NM_198177.2 Intron NP_937820.1
NM_198178.2 Intron NP_937821.2
XM_005264754.1 Intron XP_005264811.1
XM_005264755.3 Intron XP_005264812.1
XM_006713164.2 Intron XP_006713227.1
XM_011533722.2 Intron XP_011532024.1
XM_011533723.2 Intron XP_011532025.1
XM_011533725.1 Intron XP_011532027.1
XM_011533726.1 Intron XP_011532028.1
XM_017006444.1 Intron XP_016861933.1
XM_017006445.1 Intron XP_016861934.1
XM_017006446.1 Intron XP_016861935.1
XM_017006447.1 Intron XP_016861936.1
XM_017006448.1 Intron XP_016861937.1

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