Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCCATTGGCATCACCGGTGCAGCCA[C/T]TGGTGGCAGCGGGTACCGGTCCTTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 600284 MIM: 611670 MIM: 607391 | ||||||||||||||||||||
Literature Links: |
ELL 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 |
ELL - elongation factor for RNA polymerase II | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
ISYNA1 - inositol-3-phosphate synthase 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001170938.1 | 1538 | Missense Mutation | AAT,AGT | N,S 485 | NP_001164409.1 | |
NM_001253389.1 | 1538 | Missense Mutation | AAT,AGT | N,S 411 | NP_001240318.1 | |
NM_016368.4 | 1538 | Missense Mutation | AAT,AGT | N,S 539 | NP_057452.1 | |
XM_011528059.1 | 1538 | Missense Mutation | AAT,AGT | N,S 607 | XP_011526361.1 |
SSBP4 - single stranded DNA binding protein 4 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001009998.3 | 1538 | Intron | NP_001009998.1 | |||
NM_032627.4 | 1538 | Intron | NP_116016.1 | |||
XM_005259790.3 | 1538 | Intron | XP_005259847.1 | |||
XM_006722665.3 | 1538 | Intron | XP_006722728.1 | |||
XM_006722666.2 | 1538 | Intron | XP_006722729.1 | |||
XM_006722668.2 | 1538 | Intron | XP_006722731.1 | |||
XM_017026431.1 | 1538 | Intron | XP_016881920.1 | |||
XM_017026432.1 | 1538 | Intron | XP_016881921.1 | |||
XM_017026433.1 | 1538 | Intron | XP_016881922.1 | |||
XM_017026434.1 | 1538 | Intron | XP_016881923.1 | |||
XM_017026435.1 | 1538 | Intron | XP_016881924.1 | |||
XM_017026436.1 | 1538 | Intron | XP_016881925.1 | |||
XM_017026437.1 | 1538 | Intron | XP_016881926.1 |