rs772014463 Rat Genome Database

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Variant: rs772014463 -  Homo sapiens

RGD ID: 127232080
RS ID: rs772014463
ClinVar ID: CV1071481
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LRAT  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 4 155,670,159
GRCh38 4 154,749,007
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_004744.5:c.564T>C
NG_009110.1:g.9997T>C
NP_001288574.1:p.Ile188=
NP_004735.2:p.Ile188=
More... 		01/08/2024 synonymous variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:LRAT
Accession:NM_001301645
Location:EXON
Amino Acid Prediction: I to I (synonymous)
Amino Acid Position: 188
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MKNPMLEVVSLLLEKLLLISNFTLFSSGAAGEDKGRNSFYETSSFHRGDVLEVPRTHLTHYGIYLGDNRVAHMMPDILLA
LTDDMGRTQKVVSNKRLILGVIVKVASIRVDTVEDFAYGANILVNHLDESLQKKALLNEEVARRAEKLLGFTPYSLLWNN
CEHFVTYCRYGTPISPQSDKFCETVKIIIRDQRSVLASAVLGLASIVCTGLVSYTTLPAIFIPFFLWMAG*

Gene Symbol:LRAT
Accession:NM_004744
Location:EXON
Amino Acid Prediction: I to I (synonymous)
Amino Acid Position: 188
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MKNPMLEVVSLLLEKLLLISNFTLFSSGAAGEDKGRNSFYETSSFHRGDVLEVPRTHLTHYGIYLGDNRVAHMMPDILLA
LTDDMGRTQKVVSNKRLILGVIVKVASIRVDTVEDFAYGANILVNHLDESLQKKALLNEEVARRAEKLLGFTPYSLLWNN
CEHFVTYCRYGTPISPQSDKFCETVKIIIRDQRSVLASAVLGLASIVCTGLVSYTTLPAIFIPFFLWMAG*

Gene Symbol:LRAT
Accession:XM_047416405
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001395552 CLINVAR
dbSNP (RS) rs772014463 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LRAT CLINVAR
OMIM 604863 CLINVAR