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SNP ID: rs151229168
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.11:532701 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CTCTCATCAGGAGGGTTCAGCTTCC[A/G]CAGCTTGTGCTGCCGGATCTCACGC
Phenotype: MIM: 190020
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: HRAS PubMed Links

Gene Details

Gene: HRAS
Gene Name: HRas proto-oncogene, GTPase

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001130442.2	710	Missense Mutation	CGG,TGG	R169W	NP_001123914.1
NM_001318054.1	710	Missense Mutation	CGG,TGG	R90W	NP_001304983.1
NM_005343.3	710	Missense Mutation	CGG,TGG	R169W	NP_005334.1
NM_176795.4	710	UTR 3			NP_789765.1

Gene: LOC101059906
Gene Name: collagen alpha-2(IV) chain-like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
XM_003959933.4	710	Intron			XP_003959982.2

Gene: LRRC56
Gene Name: leucine rich repeat containing 56

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_198075.3	710	Intron			NP_932341.1
XM_005252775.2	710	Intron			XP_005252832.1
XM_005252776.2	710	Intron			XP_005252833.1
XM_006718132.2	710	Intron			XP_006718195.1
XM_006718133.2	710	Intron			XP_006718196.1
XM_011519875.2	710	Intron			XP_011518177.1
XM_011519876.1	710	Intron			XP_011518178.1
XM_011519877.2	710	Intron			XP_011518179.1
XM_017017167.1	710	Intron			XP_016872656.1
XM_017017168.1	710	Intron			XP_016872657.1

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