Product Details

SNP ID
rs144725155
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:82460023 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGTAAGAAAACAAAAACTGATGACC[A/G]AGAGAATGTGTCAGCCGATGCACCG
Phenotype
MIM: 605349
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
C17orf62 PubMed Links

Gene Details

Gene
C17orf62
Gene Name
chromosome 17 open reading frame 62
There are no transcripts associated with this gene.

Gene
NARF
Gene Name
nuclear prelamin A recognition factor
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001038618.2 105 UTR 5 NP_001033707.1
NM_001083608.1 105 Missense Mutation CAA,CGA Q20R NP_001077077.1
NM_012336.3 105 Missense Mutation CAA,CGA Q20R NP_036468.1
NM_031968.2 105 Missense Mutation CAA,CGA Q20R NP_114174.1
XM_005256340.3 105 UTR 5 XP_005256397.1
XM_006722278.3 105 Missense Mutation CAA,CGA Q20R XP_006722341.1
XM_011523541.2 105 UTR 5 XP_011521843.1
XM_011523543.2 105 UTR 5 XP_011521845.1
XM_011523544.2 105 Missense Mutation CAA,CGA Q20R XP_011521846.1
XM_017024449.1 105 UTR 5 XP_016879938.1
XM_017024450.1 105 UTR 5 XP_016879939.1

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