Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCTACTGACGAGTTTGTTGAGAGCG[C/T]GAACTTTTTCTTCCAAGAGGCGGCT
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
|||||||||||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 610608 MIM: 609580 | |||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
GINS1 PubMed Links | |||||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
||||||||||||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
---|---|---|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU)
|
||||||
EAS
|
African American - Not Available | YRI (Yoruba)
|
||||||
SAS
|
Chinese - Not Available | CHB (Han Chinese)
|
||||||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
|
||||||||
AMR
|
GINS1 - GINS complex subunit 1 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
NINL - ninein like | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001318226.1 | 2471 | Missense Mutation | CCC,CTC | P,L 1017 | NP_001305155.1 | |
NM_025176.5 | 2471 | Missense Mutation | CCC,CTC | P,L 1366 | NP_079452.3 | |
XM_011529186.2 | 2471 | Missense Mutation | CCC,CTC | P,L 1454 | XP_011527488.1 | |
XM_011529187.2 | 2471 | Missense Mutation | CCC,CTC | P,L 1449 | XP_011527489.1 | |
XM_011529188.1 | 2471 | Missense Mutation | CCC,CTC | P,L 1438 | XP_011527490.1 | |
XM_011529189.1 | 2471 | Missense Mutation | CCC,CTC | P,L 1438 | XP_011527491.1 | |
XM_011529190.1 | 2471 | Missense Mutation | CCC,CTC | P,L 1371 | XP_011527492.1 | |
XM_011529191.1 | 2471 | Missense Mutation | CCC,CTC | P,L 1279 | XP_011527493.1 | |
XM_011529192.1 | 2471 | Missense Mutation | CCC,CTC | P,L 1066 | XP_011527494.1 | |
XM_011529193.1 | 2471 | Missense Mutation | CCC,CTC | P,L 1022 | XP_011527495.1 | |
XM_011529194.2 | 2471 | Missense Mutation | CCC,CTC | P,L 1004 | XP_011527496.1 | |
XM_011529195.2 | 2471 | Missense Mutation | CCC,CTC | P,L 947 | XP_011527497.1 | |
XM_011529197.2 | 2471 | Missense Mutation | CCC,CTC | P,L 813 | XP_011527499.1 | |
XM_011529198.1 | 2471 | Missense Mutation | CCC,CTC | P,L 795 | XP_011527500.1 | |
XM_017027732.1 | 2471 | Missense Mutation | CCC,CTC | P,L 1454 | XP_016883221.1 | |
XM_017027733.1 | 2471 | Missense Mutation | CCC,CTC | P,L 1274 | XP_016883222.1 | |
XM_017027734.1 | 2471 | Missense Mutation | CCC,CTC | P,L 880 | XP_016883223.1 | |
XM_017027735.1 | 2471 | Missense Mutation | CCC,CTC | P,L 813 | XP_016883224.1 |