Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGGTCTGTCCACAGATGTGATGGTG[A/C]TTCTCCCAGTCTTTGTGCTGGCAAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 133435 | ||||||||||||||||||||
Literature Links: |
RUNX1T1 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
RUNX1T1 - RUNX1 translocation partner 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001198625.1 | 1902 | Missense Mutation | AAG,AAT | K,N 519 | NP_001185554.1 | |
NM_001198626.1 | 1902 | Missense Mutation | AAG,AAT | K,N 546 | NP_001185555.1 | |
NM_001198627.1 | 1902 | Missense Mutation | AAG,AAT | K,N 546 | NP_001185556.1 | |
NM_001198628.1 | 1902 | Missense Mutation | AAG,AAT | K,N 546 | NP_001185557.1 | |
NM_001198629.1 | 1902 | Missense Mutation | AAG,AAT | K,N 546 | NP_001185558.1 | |
NM_001198630.1 | 1902 | Missense Mutation | AAG,AAT | K,N 546 | NP_001185559.1 | |
NM_001198631.1 | 1902 | Missense Mutation | AAG,AAT | K,N 546 | NP_001185560.1 | |
NM_001198632.1 | 1902 | Missense Mutation | AAG,AAT | K,N 519 | NP_001185561.1 | |
NM_001198633.1 | 1902 | Missense Mutation | AAG,AAT | K,N 526 | NP_001185562.1 | |
NM_001198634.1 | 1902 | Missense Mutation | AAG,AAT | K,N 557 | NP_001185563.1 | |
NM_001198679.1 | 1902 | Missense Mutation | AAG,AAT | K,N 605 | NP_001185608.1 | |
NM_004349.3 | 1902 | Missense Mutation | AAG,AAT | K,N 519 | NP_004340.1 | |
NM_175634.2 | 1902 | Missense Mutation | AAG,AAT | K,N 546 | NP_783552.1 | |
NM_175635.2 | 1902 | Missense Mutation | AAG,AAT | K,N 509 | NP_783553.1 | |
NM_175636.2 | 1902 | Missense Mutation | AAG,AAT | K,N 509 | NP_783554.1 | |
XM_006716676.3 | 1902 | Missense Mutation | AAG,AAT | K,N 509 | XP_006716739.1 | |
XM_011517351.2 | 1902 | Missense Mutation | AAG,AAT | K,N 546 | XP_011515653.1 | |
XM_011517352.2 | 1902 | Missense Mutation | AAG,AAT | K,N 519 | XP_011515654.1 | |
XM_011517353.2 | 1902 | Missense Mutation | AAG,AAT | K,N 509 | XP_011515655.1 | |
XM_017013930.1 | 1902 | Missense Mutation | AAG,AAT | K,N 574 | XP_016869419.1 | |
XM_017013931.1 | 1902 | Missense Mutation | AAG,AAT | K,N 546 | XP_016869420.1 | |
XM_017013932.1 | 1902 | Missense Mutation | AAG,AAT | K,N 519 | XP_016869421.1 | |
XM_017013933.1 | 1902 | Missense Mutation | AAG,AAT | K,N 519 | XP_016869422.1 | |
XM_017013934.1 | 1902 | Missense Mutation | AAG,AAT | K,N 509 | XP_016869423.1 | |
XM_017013935.1 | 1902 | Missense Mutation | AAG,AAT | K,N 509 | XP_016869424.1 | |
XM_017013936.1 | 1902 | Missense Mutation | AAG,AAT | K,N 509 | XP_016869425.1 | |
XM_017013937.1 | 1902 | Missense Mutation | AAG,AAT | K,N 509 | XP_016869426.1 | |
XM_017013938.1 | 1902 | Intron | XP_016869427.1 | |||
XM_017013939.1 | 1902 | Missense Mutation | AAG,AAT | K,N 324 | XP_016869428.1 | |
XM_017013940.1 | 1902 | Missense Mutation | AAG,AAT | K,N 324 | XP_016869429.1 | |
XM_017013941.1 | 1902 | Missense Mutation | AAG,AAT | K,N 303 | XP_016869430.1 |