Product Details

SNP ID

rs140914557

Assay Type

Functionally tested

NCBI dbSNP Submissions

7

Location

Chr.1:21598029 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATCTCGGGACACGCAGGGTCCCCCA[A/G]CTTGCCGGCGTCTGGGTGGGGTGAT

Phenotype

MIM: 600278

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

RAP1GAP PubMed Links

Gene Details

Gene

RAP1GAP

Gene Name

RAP1 GTPase activating protein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001145657.1	2173	Silent Mutation	CTG,TTG	L657L	NP_001139129.1
NM_001145658.1	2173	Silent Mutation	CTG,TTG	L703L	NP_001139130.1
NM_002885.2	2173	Silent Mutation	CTG,TTG	L639L	NP_002876.2
XM_005245955.3	2173	Silent Mutation	CTG,TTG	L657L	XP_005246012.2
XM_006710804.2	2173	Silent Mutation	CTG,TTG	L724L	XP_006710867.2
XM_006710805.2	2173	Silent Mutation	CTG,TTG	L716L	XP_006710868.2
XM_017001965.1	2173	Silent Mutation	CTG,TTG	L724L	XP_016857454.1
XM_017001966.1	2173	Silent Mutation	CTG,TTG	L716L	XP_016857455.1
XM_017001967.1	2173	Silent Mutation	CTG,TTG	L686L	XP_016857456.1
XM_017001968.1	2173	Silent Mutation	CTG,TTG	L665L	XP_016857457.1
XM_017001969.1	2173	Silent Mutation	CTG,TTG	L665L	XP_016857458.1
XM_017001970.1	2173	Silent Mutation	CTG,TTG	L657L	XP_016857459.1
XM_017001971.1	2173	Silent Mutation	CTG,TTG	L780L	XP_016857460.1
XM_017001972.1	2173	Silent Mutation	CTG,TTG	L631L	XP_016857461.1
XM_017001973.1	2173	Silent Mutation	CTG,TTG	L639L	XP_016857462.1
XM_017001974.1	2173	Silent Mutation	CTG,TTG	L627L	XP_016857463.1
XM_017001975.1	2173	Silent Mutation	CTG,TTG	L631L	XP_016857464.1
XM_017001976.1	2173	Silent Mutation	CTG,TTG	L601L	XP_016857465.1
XM_017001977.1	2173	Silent Mutation	CTG,TTG	L593L	XP_016857466.1
XM_017001978.1	2173	Silent Mutation	CTG,TTG	L724L	XP_016857467.1
XM_017001979.1	2173	Silent Mutation	CTG,TTG	L716L	XP_016857468.1
XM_017001980.1	2173	Silent Mutation	CTG,TTG	L695L	XP_016857469.1
XM_017001981.1	2173	Silent Mutation	CTG,TTG	L665L	XP_016857470.1
XM_017001982.1	2173	Silent Mutation	CTG,TTG	L665L	XP_016857471.1
XM_017001983.1	2173	Silent Mutation	CTG,TTG	L665L	XP_016857472.1
XM_017001984.1	2173	Silent Mutation	CTG,TTG	L657L	XP_016857473.1
XM_017001985.1	2173	Silent Mutation	CTG,TTG	L657L	XP_016857474.1
XM_017001986.1	2173	Silent Mutation	CTG,TTG	L639L	XP_016857475.1
XM_017001987.1	2173	Silent Mutation	CTG,TTG	L639L	XP_016857476.1
XM_017001988.1	2173	Silent Mutation	CTG,TTG	L639L	XP_016857477.1
XM_017001989.1	2173	Silent Mutation	CTG,TTG	L631L	XP_016857478.1
XM_017001990.1	2173	Silent Mutation	CTG,TTG	L631L	XP_016857479.1
XM_017001991.1	2173	Silent Mutation	CTG,TTG	L601L	XP_016857480.1

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