Product Details

SNP ID

rs142489118

Assay Type

Functionally tested

NCBI dbSNP Submissions

14

Location

Chr.1:98663616 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAAATGACAGGTCCCGACCAGAAGC[A/G]TTTCTAAATAAGCATTTCTGGTGAA

Phenotype

MIM: 614904

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SNX7 PubMed Links

Gene Details

Gene

SNX7

Gene Name

sorting nexin 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015976.4		Intron			NP_057060.2
NM_152238.3		Intron			NP_689424.2
XM_006710677.2		Intron			XP_006710740.1
XM_006710678.2		Intron			XP_006710741.1
XM_011541564.2		Intron			XP_011539866.1
XM_017001425.1		Intron			XP_016856914.1
XM_017001426.1		Intron			XP_016856915.1
XM_017001427.1		Intron			XP_016856916.1
XM_017001428.1		Intron			XP_016856917.1

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