Product Details

SNP ID

rs200598460

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:47274569 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTGTCTTTATGTTCTTCAGGCACCC[A/G]AGCAGTGATAGCGTGGCCCAGACTC

Phenotype

MIM: 603584 MIM: 602423

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

LOC101928943 PubMed Links

Gene Details

Gene

LOC101928943

Gene Name

uncharacterized LOC101928943

There are no transcripts associated with this gene.

Gene

MADD

Gene Name

MAP kinase activating death domain

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001135943.1	284	Silent Mutation	CCA,CCG	P23P	NP_001129415.1
NM_001135944.1	284	Silent Mutation	CCA,CCG	P23P	NP_001129416.1
NM_003682.3	284	Silent Mutation	CCA,CCG	P23P	NP_003673.3
NM_130470.2	284	Silent Mutation	CCA,CCG	P23P	NP_569826.2
NM_130471.2	284	Silent Mutation	CCA,CCG	P23P	NP_569827.2
NM_130472.2	284	Silent Mutation	CCA,CCG	P23P	NP_569828.2
NM_130473.2	284	Silent Mutation	CCA,CCG	P23P	NP_569829.2
NM_130474.2	284	Silent Mutation	CCA,CCG	P23P	NP_569830.2
NM_130475.2	284	Silent Mutation	CCA,CCG	P23P	NP_569831.1
NM_130476.2	284	Silent Mutation	CCA,CCG	P23P	NP_569832.2
XM_005253189.2	284	Silent Mutation	CCA,CCG	P23P	XP_005253246.1
XM_005253196.2	284	Silent Mutation	CCA,CCG	P23P	XP_005253253.1
XM_005253199.2	284	Silent Mutation	CCA,CCG	P23P	XP_005253256.1
XM_005253200.2	284	Silent Mutation	CCA,CCG	P23P	XP_005253257.1
XM_005253201.2	284	Silent Mutation	CCA,CCG	P23P	XP_005253258.1
XM_005253203.2	284	Silent Mutation	CCA,CCG	P23P	XP_005253260.1
XM_005253204.2	284	Silent Mutation	CCA,CCG	P23P	XP_005253261.1
XM_005253205.1	284	Silent Mutation	CCA,CCG	P23P	XP_005253262.1
XM_017018478.1	284	Silent Mutation	CCA,CCG	P23P	XP_016873967.1
XM_017018479.1	284	Silent Mutation	CCA,CCG	P23P	XP_016873968.1
XM_017018480.1	284	Silent Mutation	CCA,CCG	P23P	XP_016873969.1
XM_017018481.1	284	Silent Mutation	CCA,CCG	P23P	XP_016873970.1
XM_017018482.1	284	Silent Mutation	CCA,CCG	P23P	XP_016873971.1
XM_017018483.1	284	Silent Mutation	CCA,CCG	P23P	XP_016873972.1
XM_017018484.1	284	Silent Mutation	CCA,CCG	P23P	XP_016873973.1
XM_017018485.1	284	Silent Mutation	CCA,CCG	P23P	XP_016873974.1
XM_017018486.1	284	Silent Mutation	CCA,CCG	P23P	XP_016873975.1
XM_017018487.1	284	Silent Mutation	CCA,CCG	P23P	XP_016873976.1
XM_017018488.1	284	Silent Mutation	CCA,CCG	P23P	XP_016873977.1
XM_017018489.1	284	Silent Mutation	CCA,CCG	P23P	XP_016873978.1
XM_017018490.1	284	Silent Mutation	CCA,CCG	P23P	XP_016873979.1
XM_017018491.1	284	Silent Mutation	CCA,CCG	P23P	XP_016873980.1
XM_017018492.1	284	Silent Mutation	CCA,CCG	P23P	XP_016873981.1
XM_017018493.1	284	Silent Mutation	CCA,CCG	P23P	XP_016873982.1
XM_017018494.1	284	Silent Mutation	CCA,CCG	P23P	XP_016873983.1
XM_017018495.1	284	Silent Mutation	CCA,CCG	P23P	XP_016873984.1
XM_017018496.1	284	Silent Mutation	CCA,CCG	P23P	XP_016873985.1
XM_017018497.1	284	Silent Mutation	CCA,CCG	P23P	XP_016873986.1
XM_017018498.1	284	Silent Mutation	CCA,CCG	P23P	XP_016873987.1
XM_017018499.1	284	Silent Mutation	CCA,CCG	P23P	XP_016873988.1
XM_017018500.1	284	Silent Mutation	CCA,CCG	P23P	XP_016873989.1
XM_017018501.1	284	Silent Mutation	CCA,CCG	P23P	XP_016873990.1
XM_017018502.1	284	Silent Mutation	CCA,CCG	P23P	XP_016873991.1
XM_017018503.1	284	Silent Mutation	CCA,CCG	P23P	XP_016873992.1
XM_017018504.1	284	Silent Mutation	CCA,CCG	P23P	XP_016873993.1
XM_017018505.1	284	Silent Mutation	CCA,CCG	P23P	XP_016873994.1
XM_017018506.1	284	Silent Mutation	CCA,CCG	P23P	XP_016873995.1
XM_017018507.1	284	Silent Mutation	CCA,CCG	P23P	XP_016873996.1
XM_017018508.1	284	Silent Mutation	CCA,CCG	P23P	XP_016873997.1
XM_017018509.1	284	Silent Mutation	CCA,CCG	P23P	XP_016873998.1
XM_017018510.1	284	Silent Mutation	CCA,CCG	P23P	XP_016873999.1

Gene

NR1H3

Gene Name

nuclear receptor subfamily 1 group H member 3

There are no transcripts associated with this gene.

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