rs61730810 Rat Genome Database

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Variant: rs61730810 -  Homo sapiens

RGD ID: 15177817
RS ID: rs61730810
ClinVar ID: CV729167
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TXN2  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 22 36,876,852
GRCh38 22 36,480,805
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.33G>A
NG_046718.1:g.5836G>A
NC_000022.11:g.36480805C>T
NC_000022.10:g.36876852C>T
More... 		01/22/2024 synonymous variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TXN2
Accession:NM_012473
Location:EXON
Amino Acid Prediction: L to L (synonymous)
Amino Acid Position: 11
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MAQRLLLRRFLASVISRKPSQGQWPPLTSRALQTPQCSPGGLTVTPNPARTIYTTRISLTTFNIQDGPDFQDRVVNSETP
VVVDFHAQWCGPCKILGPRLEKMVAKQHGKVVMAKVDIDDHTDLAIEYEVSAVPTVLAMKNGDVVDKFVGIKDEDQLEAF
LKKLIG*

Gene Symbol:TXN2
Accession:XM_006724226
Location:EXON
Amino Acid Prediction: L to L (synonymous)
Amino Acid Position: 11
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MAQRLLLRRFLASVISRKPSQGQWPPLTSRALQTPQCSPGGLTVTPNPARTIYTTRISLTTFNIQDGPDFQDRVVNSETP
VVVDFHAQWCGPCKILGPRLEKMVAKQHGKVVMAKVDIDDHTDLAIEYEVSAVPTVLAMKNGDVVDKFVGIKDEDQLEAF
LKKLIG*
Variant Samples
Additional References at PubMed
PMID:25741868   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000884916 CLINVAR
dbSNP (RS) rs61730810 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TXN2 CLINVAR
OMIM 609063 CLINVAR