RGD:156445945 Rat Genome Database

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Variant: RGD:156445945 -  Homo sapiens

RGD ID: 156445945
ClinVar ID: CV1950969
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TXN2  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 22 36,863,923
GRCh38 22 36,467,876
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_012473.4:c.429C>T
NG_046718.1:g.18765C>T
NC_000022.11:g.36467876G>A
NC_000022.10:g.36863923G>A
More... 		07/13/2022 synonymous variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TXN2
Accession:NM_012473
Location:EXON
Amino Acid Prediction: D to D (synonymous)
Amino Acid Position: 143
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MAQRLLLRRFLASVISRKPSQGQWPPLTSRALQTPQCSPGGLTVTPNPARTIYTTRISLTTFNIQDGPDFQDRVVNSETP
VVVDFHAQWCGPCKILGPRLEKMVAKQHGKVVMAKVDIDDHTDLAIEYEVSAVPTVLAMKNGDVVDKFVGIKDEDQLEAF
LKKLIG*

Gene Symbol:TXN2
Accession:XM_006724226
Location:EXON
Amino Acid Prediction: D to D (synonymous)
Amino Acid Position: 143
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MAQRLLLRRFLASVISRKPSQGQWPPLTSRALQTPQCSPGGLTVTPNPARTIYTTRISLTTFNIQDGPDFQDRVVNSETP
VVVDFHAQWCGPCKILGPRLEKMVAKQHGKVVMAKVDIDDHTDLAIEYEVSAVPTVLAMKNGDVVDKFVGIKDEDQLEAF
LKKLIG*
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003116908 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TXN2 CLINVAR
OMIM 609063 CLINVAR