Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TAGCTGCCCCCTGCAGGCCTTACCT[C/G]GCTGGGGCGCGCTGTACAGATCTTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 604126 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SVIL PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
SVIL - supervillin | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001323599.1 | 6884 | Missense Mutation | CCA,CGA | P,R 1734 | NP_001310528.1 | |
NM_001323600.1 | 6884 | Missense Mutation | CCA,CGA | P,R 1650 | NP_001310529.1 | |
NM_003174.3 | 6884 | Missense Mutation | CCA,CGA | P,R 1618 | NP_003165.2 | |
NM_021738.2 | 6884 | Missense Mutation | CCA,CGA | P,R 2044 | NP_068506.2 | |
XM_005252570.2 | 6884 | Missense Mutation | CCA,CGA | P,R 2086 | XP_005252627.1 | |
XM_005252571.3 | 6884 | Missense Mutation | CCA,CGA | P,R 2086 | XP_005252628.1 | |
XM_005252573.2 | 6884 | Missense Mutation | CCA,CGA | P,R 2086 | XP_005252630.1 | |
XM_011519630.2 | 6884 | Missense Mutation | CCA,CGA | P,R 2145 | XP_011517932.2 | |
XM_011519631.2 | 6884 | Missense Mutation | CCA,CGA | P,R 2139 | XP_011517933.2 | |
XM_011519632.2 | 6884 | Missense Mutation | CCA,CGA | P,R 2114 | XP_011517934.2 | |
XM_011519633.2 | 6884 | Missense Mutation | CCA,CGA | P,R 2097 | XP_011517935.2 | |
XM_011519634.1 | 6884 | Missense Mutation | CCA,CGA | P,R 2086 | XP_011517936.1 | |
XM_011519635.1 | 6884 | Missense Mutation | CCA,CGA | P,R 2086 | XP_011517937.1 | |
XM_011519636.2 | 6884 | Missense Mutation | CCA,CGA | P,R 1861 | XP_011517938.2 | |
XM_011519637.2 | 6884 | Missense Mutation | CCA,CGA | P,R 1777 | XP_011517939.2 | |
XM_011519638.2 | 6884 | Missense Mutation | CCA,CGA | P,R 1745 | XP_011517940.2 | |
XM_017016575.1 | 6884 | Missense Mutation | CCA,CGA | P,R 2171 | XP_016872064.1 | |
XM_017016576.1 | 6884 | Missense Mutation | CCA,CGA | P,R 2144 | XP_016872065.1 | |
XM_017016577.1 | 6884 | Missense Mutation | CCA,CGA | P,R 2129 | XP_016872066.1 | |
XM_017016578.1 | 6884 | Missense Mutation | CCA,CGA | P,R 1829 | XP_016872067.1 | |
XM_017016579.1 | 6884 | Missense Mutation | CCA,CGA | P,R 1819 | XP_016872068.1 | |
XM_017016580.1 | 6884 | Missense Mutation | CCA,CGA | P,R 1804 | XP_016872069.1 | |
XM_017016581.1 | 6884 | Missense Mutation | CCA,CGA | P,R 1735 | XP_016872070.1 | |
XM_017016582.1 | 6884 | Missense Mutation | CCA,CGA | P,R 1703 | XP_016872071.1 | |
XM_017016583.1 | 6884 | Intron | XP_016872072.1 |
SVIL-AS1 - SVIL antisense RNA 1 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |