RGD:156028848 Rat Genome Database

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Variant: RGD:156028848 -  Homo sapiens

RGD ID: 156028848
ClinVar ID: CV2205867
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC105369309  LRRC55  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 11 56,949,774
GRCh38 11 57,182,300
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001005210.4:c.278T>G
NG_079302.1:g.46T>G
NC_000011.10:g.57182300T>G
NC_000011.9:g.56949774T>G
More... 		12/28/2022 missense variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:LRRC55
Accession:NM_001005210
Location:EXON
Amino Acid Prediction: V to G (nonsynonymous)
Amino Acid Position: 93
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MGDTWAQLPWPGPPHPAMLLISLLLAAGLMHSDAGTSCPVLCTCRNQVVDCSSQRLFSVPPDLPMDTRNLSLAHNRITAV
PPGYLTCYMELQGLDLHNNSLMELPRGLFLHAKRLAHLDLSYNNFSHVPADMFQEAHGLVHIDLSHNPWLRRVHPQAFQG
LMQLRDLDLSYGGLAFLSLEALEGLPGLVTLQIGGNPWVCGCTMEPLLKWLRNRIQRCTADSQLAECRGPPEVEGAPLFS
LTEESFKACHLTLTLDDYLFIAFVGFVVSIASVATNFLLGITANCCHRWSKASEEEEI*

Gene Symbol:LOC105369309
Accession:XR_950120
Location:INTRON;NON-CODING

Gene Symbol:LOC105369309
Accession:XR_001748217
Location:INTRON;NON-CODING

Gene Symbol:LOC105369309
Accession:XR_007062670
Location:INTRON;NON-CODING

Gene Symbol:LOC105369309
Accession:XR_007062671
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV002691423 CLINVAR
MedGen C0950123 CLINVAR
NCBI Gene LRRC55 CLINVAR
OMIM 615213 CLINVAR