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TTTTGTCAAAGTCCTGGAGTCTCTC[A/G]CTGAACTTGGAAGCAATTTCTGTAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600934 | ||||||||||||||||||||
Literature Links: |
FOLH1 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 |
FOLH1 - folate hydrolase (prostate-specific membrane antigen) 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001014986.1 | 2202 | Silent Mutation | AGC,AGT | S,S 647 | NP_001014986.1 | |
NM_001193471.1 | 2202 | Silent Mutation | AGC,AGT | S,S 632 | NP_001180400.1 | |
NM_001193472.1 | 2202 | Silent Mutation | AGC,AGT | S,S 632 | NP_001180401.1 | |
NM_001193473.1 | 2202 | Silent Mutation | AGC,AGT | S,S 339 | NP_001180402.1 | |
NM_004476.1 | 2202 | Silent Mutation | AGC,AGT | S,S 647 | NP_004467.1 | |
XM_011519958.2 | 2202 | Intron | XP_011518260.2 | |||
XM_017017432.1 | 2202 | Silent Mutation | AGC,AGT | S,S 702 | XP_016872921.1 | |
XM_017017433.1 | 2202 | Silent Mutation | AGC,AGT | S,S 702 | XP_016872922.1 | |
XM_017017434.1 | 2202 | Intron | XP_016872923.1 | |||
XM_017017435.1 | 2202 | Intron | XP_016872924.1 | |||
XM_017017436.1 | 2202 | Silent Mutation | AGC,AGT | S,S 590 | XP_016872925.1 | |
XM_017017437.1 | 2202 | Intron | XP_016872926.1 | |||
XM_017017438.1 | 2202 | Silent Mutation | AGC,AGT | S,S 590 | XP_016872927.1 | |
XM_017017439.1 | 2202 | Intron | XP_016872928.1 | |||
XM_017017440.1 | 2202 | Intron | XP_016872929.1 | |||
XM_017017441.1 | 2202 | Intron | XP_016872930.1 | |||
XM_017017442.1 | 2202 | Intron | XP_016872931.1 | |||
XM_017017443.1 | 2202 | Intron | XP_016872932.1 | |||
XM_017017444.1 | 2202 | Silent Mutation | AGC,AGT | S,S 339 | XP_016872933.1 | |
XM_017017445.1 | 2202 | Silent Mutation | AGC,AGT | S,S 339 | XP_016872934.1 | |
XM_017017446.1 | 2202 | Silent Mutation | AGC,AGT | S,S 339 | XP_016872935.1 | |
XM_017017447.1 | 2202 | Intron | XP_016872936.1 | |||
XM_017017448.1 | 2202 | Intron | XP_016872937.1 | |||
XM_017017449.1 | 2202 | Silent Mutation | AGC,AGT | S,S 339 | XP_016872938.1 | |
XM_017017450.1 | 2202 | Silent Mutation | AGC,AGT | S,S 339 | XP_016872939.1 | |
XM_017017451.1 | 2202 | Intron | XP_016872940.1 |