Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGATTTTCAACCTGGAAGACGATAC[C/T]GCAGAAGCTGTGCCCCTAGAAAGAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610008 MIM: 188830 MIM: 609224 | ||||||||||||||||||||
Literature Links: |
ARSG 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 |
ARSG - arylsulfatase G | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001267727.1 | 2290 | Silent Mutation | ACC,ACT | T,T 462 | NP_001254656.1 | |
NM_014960.4 | 2290 | Silent Mutation | ACC,ACT | T,T 462 | NP_055775.2 | |
XM_005257170.3 | 2290 | Silent Mutation | ACC,ACT | T,T 462 | XP_005257227.1 | |
XM_005257172.3 | 2290 | Intron | XP_005257229.1 | |||
XM_006721777.3 | 2290 | Silent Mutation | ACC,ACT | T,T 489 | XP_006721840.2 | |
XM_006721779.3 | 2290 | Intron | XP_006721842.1 | |||
XM_011524535.2 | 2290 | Silent Mutation | ACC,ACT | T,T 489 | XP_011522837.1 | |
XM_011524536.2 | 2290 | Silent Mutation | ACC,ACT | T,T 489 | XP_011522838.1 | |
XM_011524537.1 | 2290 | Silent Mutation | ACC,ACT | T,T 489 | XP_011522839.1 | |
XM_011524538.2 | 2290 | Silent Mutation | ACC,ACT | T,T 489 | XP_011522840.1 | |
XM_011524540.2 | 2290 | Silent Mutation | ACC,ACT | T,T 488 | XP_011522842.1 | |
XM_011524541.2 | 2290 | Intron | XP_011522843.1 | |||
XM_011524542.2 | 2290 | Intron | XP_011522844.1 | |||
XM_011524543.2 | 2290 | Intron | XP_011522845.1 | |||
XM_011524544.2 | 2290 | Intron | XP_011522846.1 | |||
XM_011524545.2 | 2290 | UTR 3 | XP_011522847.1 | |||
XM_011524546.2 | 2290 | Silent Mutation | ACC,ACT | T,T 240 | XP_011522848.1 | |
XM_017024360.1 | 2290 | Silent Mutation | ACC,ACT | T,T 489 | XP_016879849.1 | |
XM_017024361.1 | 2290 | Silent Mutation | ACC,ACT | T,T 462 | XP_016879850.1 | |
XM_017024362.1 | 2290 | Silent Mutation | ACC,ACT | T,T 462 | XP_016879851.1 | |
XM_017024363.1 | 2290 | Silent Mutation | ACC,ACT | T,T 462 | XP_016879852.1 | |
XM_017024364.1 | 2290 | Silent Mutation | ACC,ACT | T,T 462 | XP_016879853.1 | |
XM_017024365.1 | 2290 | Silent Mutation | ACC,ACT | T,T 462 | XP_016879854.1 | |
XM_017024366.1 | 2290 | Intron | XP_016879855.1 | |||
XM_017024367.1 | 2290 | Intron | XP_016879856.1 | |||
XM_017024368.1 | 2290 | UTR 3 | XP_016879857.1 |
MIR635 - microRNA 635 | ||||||
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There are no transcripts associated with this gene. |
PRKAR1A - protein kinase cAMP-dependent type I regulatory subunit alpha | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001276289.1 | 2290 | Intron | NP_001263218.1 | |||
NM_001276290.1 | 2290 | Intron | NP_001263219.1 | |||
NM_001278433.1 | 2290 | Intron | NP_001265362.1 | |||
NM_002734.4 | 2290 | Intron | NP_002725.1 | |||
NM_212471.2 | 2290 | Intron | NP_997636.1 | |||
NM_212472.2 | 2290 | Intron | NP_997637.1 | |||
XM_011524983.2 | 2290 | Intron | XP_011523285.1 | |||
XM_011524984.2 | 2290 | Intron | XP_011523286.1 | |||
XM_011524985.2 | 2290 | Intron | XP_011523287.1 |
WIPI1 - WD repeat domain, phosphoinositide interacting 1 | ||||||
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There are no transcripts associated with this gene. |