rs139122017 Rat Genome Database

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Variant: rs139122017 -  Homo sapiens

RGD ID: 150482880
RS ID: rs139122017
ClinVar ID: CV1261691
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC127815202  ROR2  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 9 94,711,949
GRCh38 9 91,949,667
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001318204.2:c.97+200C>A
NM_004560.4:c.97+200C>A
NG_008089.1:g.5496C>A
NC_000009.12:g.91949667G>T
More... 		11/23/2019 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ROR2
Accession:NM_004560
Location:INTRON

Gene Symbol:ROR2
Accession:XM_005252008
Location:INTRON

Gene Symbol:ROR2
Accession:XM_005252009
Location:INTRON

Gene Symbol:ROR2
Accession:XM_006717121
Location:INTRON

Gene Symbol:ROR2
Accession:NM_001318204
Location:INTRON

Gene Symbol:ROR2
Accession:XM_017014762
Location:INTRON

Gene Symbol:ROR2
Accession:XM_047423436
Location:INTRON

Gene Symbol:ROR2
Accession:XM_047423435
Location:INTRON

Gene Symbol:ROR2
Accession:XM_047423437
Location:INTRON

Gene Symbol:ROR2
Accession:XM_047423434
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001686295 CLINVAR
dbSNP (RS) rs139122017 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ROR2 CLINVAR
OMIM 602337 CLINVAR