RGD:126758009 Rat Genome Database

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Variant: RGD:126758009 -  Homo sapiens

RGD ID: 126758009
RS ID: rs568826131
ClinVar ID: CV994611
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: B3GAT3  LOC127821279  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 11 62,389,388
GRCh38 11 62,621,916
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001288721.2:c.-229C>T
NM_001288722.2:c.32C>T
NM_001288723.2:c.32C>T
NM_012200.4:c.32C>T
More... 		05/20/2020 5 prime utr variant uncertain significance LARSEN SYNDROME, AUTOSOMAL RECESSIVE; MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS; Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:B3GAT3
Accession:NM_001288721
Location:5UTRS;EXON

Gene Symbol:B3GAT3
Accession:NM_012200
Location:EXON
Amino Acid Prediction: A to V (nonsynonymous)
Amino Acid Position: 11
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MKLKLKNVFLVYFLVSIAGLLYALVQLGQPCDCLPPLRAAAEQLRQKDLRISQLQAELRRPPPAPAQPPEPEALPTIYVV
TPTYARLVQKAELVRLSQTLSLVPRLHWLLVEDAEGPTPLVSGLLAASGLLFTHLVVLTPKAQRLREGEPGWVHPRGVEQ
RNKALDWLRGRGGAVGGEKDPPPPGTQGVVYFADDDNTYSRELFEEMRWTRGVSVWPVGLVGGLRFEGPQVQDGRVVGFH
TAWEPSRPFPVDMAGFAVALPLLLDKPNAQFDSTAPRGHLESSLLSHLVDPKDLEPRAANCTRVLVWHTRTEKPKMKQEE
QLQRQGRGSDPAIEV*

Gene Symbol:B3GAT3
Accession:NM_001288723
Location:EXON
Amino Acid Prediction: A to V (nonsynonymous)
Amino Acid Position: 11
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MKLKLKNVFLVYFLVSIAGLLYALVQLGQPCDCLPPLRAAAEQLRQKDLRISQLQAELRRPPPAPAQPPEPEALPTIYVV
TPTYARLVQKAELVRLSQTLSLVPRLHWLLVEDAEGPTPLVSGLLAASGLLFTHLVVLTPKAQRLREGEPGWVHPRGVEQ
RNKALDWLRGRGGAVGGEKDPPPPGTQGVVYFADDDNTYSRELFEEMRWTRGVSVWPVGLVGGLRFEGPQVQDGRVVGFH
TAWEPSRPFPVDMAGFAVALPLLLDKPNAQFDSTAPRGHLESSLLSHLVDPKDLEPRAANCTRTESRCVTQAGVQ*

Gene Symbol:B3GAT3
Accession:NM_001288722
Location:EXON
Amino Acid Prediction: A to V (nonsynonymous)
Amino Acid Position: 11
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MKLKLKNVFLVYFLVSIAGLLYALVQLGQPCDCLPPLRAAAEQLRQKDLRISQLQAELRRPPPAPAQPPEPEALPTIYVV
TPTYARLVQKAELVRLSQTLSLVPRLHWLLVEDAEGPTPLVSGLLAASGLLFTHLVVLTPKAQRLREGEPGWVHPRGVEQ
RNKALDWLRGRGGAVGGEKDPPPPGTQGVVYFADDDNTYSRELFEEMRWTRGVSVWPVGLVGGLRFEGPQVQDGRVVGFH
TAWEPSRPFPVDMAGFAVALPLLLDKPNAQFDSTAPRGHLESSLLSHLVDPKDLEPRAANCTRSLAVSPRLECSSAILA*

Gene Symbol:B3GAT3
Accession:NR_109991
Location:EXON;NON-CODING

Gene Symbol:B3GAT3
Accession:XM_047426751
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001308588 CLINVAR
dbSNP (RS) rs568826131 CLINVAR
MedGen C3278404 CLINVAR
NCBI Gene B3GAT3 CLINVAR
OMIM 245600 CLINVAR
  606374 CLINVAR