Product Details

SNP ID
rs79588969
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.15:56920582 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TAAGGGCCCACTGCTTTTATTTTTA[A/G]TGGGTTTAATTCCTTTATTAACTGC
Phenotype
MIM: 600480
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
LOC145783 PubMed Links

Gene Details

Gene
LOC145783
Gene Name
uncharacterized LOC145783
There are no transcripts associated with this gene.

Gene
TCF12
Gene Name
transcription factor 12
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001306219.2 Intron NP_001293148.1
NM_001306220.2 Intron NP_001293149.1
NM_001322151.1 Intron NP_001309080.1
NM_001322152.1 Intron NP_001309081.1
NM_001322154.1 Intron NP_001309083.1
NM_001322156.1 Intron NP_001309085.1
NM_001322157.1 Intron NP_001309086.1
NM_001322158.1 Intron NP_001309087.1
NM_001322159.1 Intron NP_001309088.1
NM_001322161.1 Intron NP_001309090.1
NM_001322162.1 Intron NP_001309091.1
NM_001322164.1 Intron NP_001309093.1
NM_001322165.1 Intron NP_001309094.1
NM_003205.3 Intron NP_003196.1
NM_207036.1 Intron NP_996919.1
NM_207037.1 Intron NP_996920.1
NM_207038.1 Intron NP_996921.1
NM_207040.1 Intron NP_996923.1
XM_011521959.2 Intron XP_011520261.1
XM_011521960.2 Intron XP_011520262.1
XM_011521961.2 Intron XP_011520263.1
XM_011521962.2 Intron XP_011520264.1
XM_011521963.2 Intron XP_011520265.1
XM_011521965.1 Intron XP_011520267.1
XM_011521966.2 Intron XP_011520268.1
XM_011521967.1 Intron XP_011520269.1
XM_011521969.1 Intron XP_011520271.1
XM_017022520.1 Intron XP_016878009.1

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