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CCCTCACTGACAAGGACACTGGAGT[C/T]ACGCGATATGGCATCTGTGTTAACT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603584 MIM: 602423 | ||||||||||||||||||||
Literature Links: |
LOC101928943 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 |
LOC101928943 - uncharacterized LOC101928943 | ||||||
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There are no transcripts associated with this gene. |
MADD - MAP kinase activating death domain | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001135943.1 | 479 | Silent Mutation | GTC,GTT | V,V 88 | NP_001129415.1 | |
NM_001135944.1 | 479 | Silent Mutation | GTC,GTT | V,V 88 | NP_001129416.1 | |
NM_003682.3 | 479 | Silent Mutation | GTC,GTT | V,V 88 | NP_003673.3 | |
NM_130470.2 | 479 | Silent Mutation | GTC,GTT | V,V 88 | NP_569826.2 | |
NM_130471.2 | 479 | Silent Mutation | GTC,GTT | V,V 88 | NP_569827.2 | |
NM_130472.2 | 479 | Silent Mutation | GTC,GTT | V,V 88 | NP_569828.2 | |
NM_130473.2 | 479 | Silent Mutation | GTC,GTT | V,V 88 | NP_569829.2 | |
NM_130474.2 | 479 | Silent Mutation | GTC,GTT | V,V 88 | NP_569830.2 | |
NM_130475.2 | 479 | Silent Mutation | GTC,GTT | V,V 88 | NP_569831.1 | |
NM_130476.2 | 479 | Silent Mutation | GTC,GTT | V,V 88 | NP_569832.2 | |
XM_005253189.2 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_005253246.1 | |
XM_005253196.2 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_005253253.1 | |
XM_005253199.2 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_005253256.1 | |
XM_005253200.2 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_005253257.1 | |
XM_005253201.2 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_005253258.1 | |
XM_005253203.2 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_005253260.1 | |
XM_005253204.2 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_005253261.1 | |
XM_005253205.1 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_005253262.1 | |
XM_017018478.1 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_016873967.1 | |
XM_017018479.1 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_016873968.1 | |
XM_017018480.1 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_016873969.1 | |
XM_017018481.1 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_016873970.1 | |
XM_017018482.1 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_016873971.1 | |
XM_017018483.1 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_016873972.1 | |
XM_017018484.1 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_016873973.1 | |
XM_017018485.1 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_016873974.1 | |
XM_017018486.1 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_016873975.1 | |
XM_017018487.1 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_016873976.1 | |
XM_017018488.1 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_016873977.1 | |
XM_017018489.1 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_016873978.1 | |
XM_017018490.1 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_016873979.1 | |
XM_017018491.1 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_016873980.1 | |
XM_017018492.1 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_016873981.1 | |
XM_017018493.1 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_016873982.1 | |
XM_017018494.1 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_016873983.1 | |
XM_017018495.1 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_016873984.1 | |
XM_017018496.1 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_016873985.1 | |
XM_017018497.1 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_016873986.1 | |
XM_017018498.1 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_016873987.1 | |
XM_017018499.1 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_016873988.1 | |
XM_017018500.1 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_016873989.1 | |
XM_017018501.1 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_016873990.1 | |
XM_017018502.1 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_016873991.1 | |
XM_017018503.1 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_016873992.1 | |
XM_017018504.1 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_016873993.1 | |
XM_017018505.1 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_016873994.1 | |
XM_017018506.1 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_016873995.1 | |
XM_017018507.1 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_016873996.1 | |
XM_017018508.1 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_016873997.1 | |
XM_017018509.1 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_016873998.1 | |
XM_017018510.1 | 479 | Silent Mutation | GTC,GTT | V,V 88 | XP_016873999.1 |
NR1H3 - nuclear receptor subfamily 1 group H member 3 | ||||||
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There are no transcripts associated with this gene. |