RGD:407469286 Rat Genome Database

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Variant: RGD:407469286 -  Homo sapiens

RGD ID: 407469286
ClinVar ID: CV3456929
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MAS1L  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 6 29,455,631
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_052967.2:c.49G>A
NC_000006.12:g.29487854C>T
NC_000006.11:g.29455631C>T
NM_052967.1:c.49G>A
More... 		05/24/2024 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004636572 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene MAS1L CLINVAR
OMIM 607235 CLINVAR