RGD:8633631 Rat Genome Database

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Variant: RGD:8633631 -  Homo sapiens

RGD ID: 8633631
ClinVar ID: CV88846
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CXCL12  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 10 44,871,456
GRCh38 10 44,376,008
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000609.6:c.266+2629G>A
NM_001033886.2:c.291G>A
NG_016861.1:g.14090G>A
NC_000010.11:g.44376008C>T
More... 		intron|synonymous variant|intron variant not provided Malignant melanoma, somatic

Variant Details
Variant Transcripts
Gene Symbol:CXCL12
Accession:NM_001033886
Location:EXON
Amino Acid Prediction: G to G (synonymous)
Amino Acid Position: 97
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MNAKVVVVLVLVLTALCLSDGKPVSLSYRCPCRFFESHVARANVKHLKILNTPNCALQIVARLKNNNRQVCIDPKLKWIQ
EYLEKALNKGRREEKVGKKEKIGKKKRQKKRKAAQKRKN*

Gene Symbol:CXCL12
Accession:NM_001277990
Location:INTRON

Gene Symbol:CXCL12
Accession:NM_001178134
Location:INTRON

Gene Symbol:CXCL12
Accession:NM_199168
Location:INTRON

Gene Symbol:CXCL12
Accession:NM_000609
Location:INTRON

Variant Samples