RGD:8581463 Rat Genome Database

Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

Variant: RGD:8581463 -  Homo sapiens

RGD ID: 8581463
ClinVar ID: CV115902
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SYCP2L  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 6 10,956,645
GRCh38 6 10,956,412
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000006.12:g.10956412G>C
NC_000006.11:g.10956645G>C
NM_001040274.2:c.2163+170G>C
intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:SYCP2L
Accession:NM_001040274
Location:INTRON

Variant Samples