rs368840841 Rat Genome Database

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Variant: rs368840841 -  Homo sapiens

RGD ID: 15132088
RS ID: rs368840841
ClinVar ID: CV767234
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MYMK  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 9 136,380,649
GRCh38 9 133,515,527
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001080483.3:c.480C>T
NC_000009.12:g.133515527G>A
NC_000009.11:g.136380649G>A
NM_001080483.2:c.480C>T
More... 		12/31/2019 synonymous variant likely benign none provided

Gene Symbol:MYMK
Accession:NM_001080483
Location:EXON
Amino Acid Prediction: F to F (synonymous)
Amino Acid Position: 160
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MGTLVAKLLLPTLSSLAFLPTVSIAAKRRFHMEAMVYLFTLFFVALHHACNGPGLSVLCFMRHDILEYFSVYGTALSMWV
SLMALADFDEPKRSTFVMFGVLTIAVRIYHDRWGYGVYSGPIGTAILIIAAKWLQKMKEKKGLYPDKSVYTQQIGPGLCF
GALALMLRFFFEDWDYTYVHSFYHCALAMSFVLLLPKVNKKAGSPGTPAKLDCSTLCCACV*
.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV000942341 CLINVAR
dbSNP (RS) rs368840841 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MYMK CLINVAR
OMIM 615345 CLINVAR