Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CACCCTGATTGACAGCGGGGACTCC[A/G]TGGTGGCCAAGTAAGTACCAGCAGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 610695 | ||||||||||||||||||||
Literature Links: |
HSPB6 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
HSPB6 - heat shock protein family B (small) member 6 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
LIN37 - lin-37 DREAM MuvB core complex component | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
PROSER3 - proline and serine rich 3 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001039887.2 | 374 | Missense Mutation | ATG,GTG | M,V 101 | NP_001034976.2 | |
XM_011526528.1 | 374 | Missense Mutation | ATG,GTG | M,V 101 | XP_011524830.1 | |
XM_011526529.2 | 374 | Missense Mutation | ATG,GTG | M,V 101 | XP_011524831.1 | |
XM_011526530.1 | 374 | Missense Mutation | ATG,GTG | M,V 101 | XP_011524832.1 | |
XM_011526531.1 | 374 | Missense Mutation | ATG,GTG | M,V 101 | XP_011524833.1 | |
XM_011526532.1 | 374 | Missense Mutation | ATG,GTG | M,V 101 | XP_011524834.1 | |
XM_011526533.2 | 374 | Missense Mutation | ATG,GTG | M,V 101 | XP_011524835.1 | |
XM_011526534.1 | 374 | Missense Mutation | ATG,GTG | M,V 101 | XP_011524836.1 | |
XM_011526535.2 | 374 | Intron | XP_011524837.1 | |||
XM_011526536.2 | 374 | Missense Mutation | ATG,GTG | M,V 101 | XP_011524838.1 |