RGD:155963383 Rat Genome Database

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Variant: RGD:155963383 -  Homo sapiens

RGD ID: 155963383
ClinVar ID: CV2388389
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CD79B  GH-LCR  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 17 62,008,712
GRCh38 17 63,931,352
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_43t1:c.104G>A
NM_000626.4:c.101G>A
NM_021602.4:c.101G>A
NM_001039933.3:c.104G>A
More... 		08/12/2021 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Transcripts
Gene Symbol:CD79B
Accession:NM_021602
Location:EXON
Amino Acid Prediction: R to L (nonsynonymous)
Amino Acid Position: 34
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MARLALSPVPSHWMVALLLLLSAEPVPAARSEDLYRNPKGFSTLAQLKQRNTLKDGIIMIQTLLIILFIIVPIFLLLDKD
DSKAGMEEDHTYEGLDIDQTATYEDIVTLRTGEVKWSVGEHPGQE*

Gene Symbol:CD79B
Accession:NM_001329050
Location:EXON
Amino Acid Prediction: R to L (nonsynonymous)
Amino Acid Position: 35
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MARLALSPVPSHWMVALLLLLSAAEPVPAARSEDLYRNPKGFSTLAQLKQRNTLKDGIIMIQTLLIILFIIVPIFLLLDK
DDSKAGMEEDHTYEGLDIDQTATYEDIVTLRTGEVKWSVGEHPGQE*

Gene Symbol:CD79B
Accession:NM_000626
Location:EXON
Amino Acid Prediction: R to L (nonsynonymous)
Amino Acid Position: 34
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MARLALSPVPSHWMVALLLLLSAEPVPAARSEDLYRNPKGSACSRIWQSPRFIARKRGFTVKMHCYMNSASGNVSWLWKQ
EMDENPQQLKLEKGRMEESQNESLATLTIQGIRFEDNGIYFCQQKCNNTSEVYQGCGTELRVMGFSTLAQLKQRNTLKDG
IIMIQTLLIILFIIVPIFLLLDKDDSKAGMEEDHTYEGLDIDQTATYEDIVTLRTGEVKWSVGEHPGQE*

Gene Symbol:CD79B
Accession:NM_001039933
Location:EXON
Amino Acid Prediction: R to L (nonsynonymous)
Amino Acid Position: 35
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MARLALSPVPSHWMVALLLLLSAAEPVPAARSEDLYRNPKGSACSRIWQSPRFIARKRGFTVKMHCYMNSASGNVSWLWK
QEMDENPQQLKLEKGRMEESQNESLATLTIQGIRFEDNGIYFCQQKCNNTSEVYQGCGTELRVMGFSTLAQLKQRNTLKD
GIIMIQTLLIILFIIVPIFLLLDKDDSKAGMEEDHTYEGLDIDQTATYEDIVTLRTGEVKWSVGEHPGQE*
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004234838 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene CD79B CLINVAR
  GH-LCR CLINVAR
OMIM 147245 CLINVAR