Product Details

SNP ID
rs10098853
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.8:91955682 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CTTTCTCCAGACACGGGCTCATGCA[A/C]CTGCTGTGCCATCCTTGATTTTTTG
Phenotype
MIM: 133435
Polymorphism
A/C, Transversion Substitution
Allele Nomenclature
Literature Links
RUNX1T1 PubMed Links

Gene Details

Gene
RUNX1T1
Gene Name
RUNX1 translocation partner 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001198625.1 6639 UTR 3 NP_001185554.1
NM_001198626.1 6639 UTR 3 NP_001185555.1
NM_001198627.1 6639 UTR 3 NP_001185556.1
NM_001198628.1 6639 UTR 3 NP_001185557.1
NM_001198629.1 6639 UTR 3 NP_001185558.1
NM_001198630.1 6639 UTR 3 NP_001185559.1
NM_001198631.1 6639 UTR 3 NP_001185560.1
NM_001198632.1 6639 UTR 3 NP_001185561.1
NM_001198633.1 6639 UTR 3 NP_001185562.1
NM_001198634.1 6639 UTR 3 NP_001185563.1
NM_001198679.1 6639 UTR 3 NP_001185608.1
NM_004349.3 6639 UTR 3 NP_004340.1
NM_175634.2 6639 UTR 3 NP_783552.1
NM_175635.2 6639 UTR 3 NP_783553.1
NM_175636.2 6639 UTR 3 NP_783554.1
XM_006716676.3 6639 UTR 3 XP_006716739.1
XM_011517351.2 6639 UTR 3 XP_011515653.1
XM_011517352.2 6639 UTR 3 XP_011515654.1
XM_011517353.2 6639 UTR 3 XP_011515655.1
XM_017013930.1 6639 UTR 3 XP_016869419.1
XM_017013931.1 6639 UTR 3 XP_016869420.1
XM_017013932.1 6639 UTR 3 XP_016869421.1
XM_017013933.1 6639 UTR 3 XP_016869422.1
XM_017013934.1 6639 UTR 3 XP_016869423.1
XM_017013935.1 6639 UTR 3 XP_016869424.1
XM_017013936.1 6639 UTR 3 XP_016869425.1
XM_017013937.1 6639 UTR 3 XP_016869426.1
XM_017013938.1 6639 Intron XP_016869427.1
XM_017013939.1 6639 UTR 3 XP_016869428.1
XM_017013940.1 6639 UTR 3 XP_016869429.1
XM_017013941.1 6639 UTR 3 XP_016869430.1

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