Product Details

SNP ID

rs6499871

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:57193044 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATAGTCTTTCAACCAGAAAAAAATA[C/T]CTACTTTCAAAGGTGTGCTTTCTTA

Phenotype

MIM: 616585

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FAM192A PubMed Links

Gene Details

Gene

FAM192A

Gene Name

family with sequence similarity 192 member A

There are no transcripts associated with this gene.

Gene

RSPRY1

Gene Name

ring finger and SPRY domain containing 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001305163.1		Intron			NP_001292092.1
NM_001305164.1		Intron			NP_001292093.1
NM_001305182.1		Intron			NP_001292111.1
NM_133368.2		Intron			NP_588609.1
XM_005256220.1		Intron			XP_005256277.1
XM_011523427.1		Intron			XP_011521729.1
XM_011523428.1		Intron			XP_011521730.1
XM_011523430.1		Intron			XP_011521732.1
XM_017023844.1		Intron			XP_016879333.1

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