Product Details

SNP ID

rs147098824

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:89364123 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TATTTCATCTTTTTGACCTTGGTTG[C/T]CTCATCTGAAAAATAGAAATGGTAA

Phenotype

MIM: 608268

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

RRAGD PubMed Links

Gene Details

Gene

RRAGD

Gene Name

Ras related GTP binding D

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_021244.4	5464	Intron			NP_067067.1
XM_005248755.4	5464	UTR 3			XP_005248812.1
XM_011536022.2	5464	Intron			XP_011534324.1

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