rs10208616 Rat Genome Database

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Variant: rs10208616 -  Homo sapiens

RGD ID: 150438177
RS ID: rs10208616
ClinVar ID: CV1201366
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KRTCAP3  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 2 27,667,108
GRCh38 2 27,444,241
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NG_034068.1:g.50571C>T
NM_001168364.2:c.*5+180G>A
NM_001321325.2:c.*58G>A
NM_173853.4:c.*61G>A
More... 		10/31/2018 3 prime utr variant likely benign none provided

Gene Symbol:KRTCAP3
Accession:NM_173853
Location:3UTRS;EXON

Gene Symbol:KRTCAP3
Accession:NM_001321325
Location:3UTRS;EXON

Gene Symbol:KRTCAP3
Accession:XM_047443704
Location:3UTRS;EXON

Gene Symbol:KRTCAP3
Accession:NM_001168364
Location:3UTRS;INTRON

.
PMID:25741868  



Database
Acc Id
Source(s)
ClinVar RCV001583178 CLINVAR
dbSNP (RS) rs10208616 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene IFT172 CLINVAR
  KRTCAP3 CLINVAR
OMIM 607386 CLINVAR
  619261 CLINVAR