RGD:155961605 Rat Genome Database

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Variant: RGD:155961605 -  Homo sapiens

RGD ID: 155961605
ClinVar ID: CV2254227
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CYP26A1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 10 94,833,777
GRCh38 10 93,074,020
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_057157.2:c.-19+186A>G
NM_000783.4:c.86A>G
NG_008067.1:g.5546A>G
NC_000010.11:g.93074020A>G
More... 		01/10/2022 intron variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Transcripts
Gene Symbol:CYP26A1
Accession:NM_057157
Location:5UTRS;INTRON

Gene Symbol:CYP26A1
Accession:NM_000783
Location:EXON
Amino Acid Prediction: D to G (nonsynonymous)
Amino Acid Position: 29
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MGLPALLASALCTFVLPLLLFLAAIKLWGLYCVSGRDRSCALPLPPGTMGFPFFGETLQMVLQRRKFLQMKRRKYGFIYK
THLFGRPTVRVMGADNVRRILLGEHRLVSVHWPASVRTILGSGCLSNLHDSSHKQRKKVIMRAFSREALECYVPVITEEV
GSSLEQWLSCGERGLLVYPEVKRLMFRIAMRILLGCEPQLAGDGDSEQQLVEAFEEMTRNLFSLPIDVPFSGLYRGMKAR
NLIHARIEQNIRAKICGLRASEAGQGCKDALQLLIEHSWERGERLDMQALKQSSTELLFGGHETTASAATSLITYLGLYP
HVLQKVREELKSKGLLCKSNQDNKLDMEILEQLKYIGCVIKETLRLNPPVPGGFRVALKTFELNGYQIPKGWNVIYSICD
THDVAEIFTNKEEFNPDRFMLPHPEDASRFSFIPFGGGLRSCVGKEFAKILLKIFTVELARHCDWQLLNGPPTMKTSPTV
YPVDNLPARFTHFHGEI*
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004129906 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene CYP26A1 CLINVAR
OMIM 602239 CLINVAR