rs1642591589 Rat Genome Database

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Variant: rs1642591589 -  Homo sapiens

RGD ID: 151865515
RS ID: rs1642591589
ClinVar ID: CV1456021
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: C1QB  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 1 22,986,119
GRCh38 1 22,659,626
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001371184.3:c.164G>C
NM_001378156.1:c.164G>C
NM_000491.5:c.170G>C
LRG_23:g.11438G>C
More... 		09/24/2021 missense variant uncertain significance none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM

Gene Symbol:C1QB
Accession:NM_001371184
Location:EXON
Amino Acid Prediction: G to A (nonsynonymous)
Amino Acid Position: 55
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MKIPWGSIPVLMLLLLLGLIDISQAQLSCTGPPAIPGIPGIPGTPGPDGQPGTPAIKGEKGLPGLAGDHGEFGEKGDPGI
PGNPGKVGPKGPMGPKGGPGAPGAPGPKGESGDYKATQKIAFSATRTINVPLRRDQTIRFDHVITNMNNNYEPRSGKFTC
KVPGLYYFTYHASSRGNLCVNLMRGRERAQKVVTFCDYAYNTFQVTTGGMVLKLEQGENVFLQATDKNSLLGMEGANSIF
SGFLLFPDMEA*

Gene Symbol:C1QB
Accession:NM_001378156
Location:EXON
Amino Acid Prediction: G to A (nonsynonymous)
Amino Acid Position: 55
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MKIPWGSIPVLMLLLLLGLIDISQAQLSCTGPPAIPGIPGIPGTPGPDGQPGTPAIKGEKGLPGLAGDHGEFGEKGDPGI
PGNPGKVGPKGPMGPKGGPGAPGAPGPKGESGDYKATQKIAFSATRTINVPLRRDQTIRFDHVITNMNNNYEPRSGKFTC
KVPGLYYFTYHASSRGNLCVNLMRGRERAQKVVTFCDYAYNTFQVTTGGMVLKLEQGENVFLQATDKNSLLGMEGANSIF
SGFLLFPDMEA*

Gene Symbol:C1QB
Accession:NM_000491
Location:EXON
Amino Acid Prediction: G to A (nonsynonymous)
Amino Acid Position: 57
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MMMKIPWGSIPVLMLLLLLGLIDISQAQLSCTGPPAIPGIPGIPGTPGPDGQPGTPAIKGEKGLPGLAGDHGEFGEKGDP
GIPGNPGKVGPKGPMGPKGGPGAPGAPGPKGESGDYKATQKIAFSATRTINVPLRRDQTIRFDHVITNMNNNYEPRSGKF
TCKVPGLYYFTYHASSRGNLCVNLMRGRERAQKVVTFCDYAYNTFQVTTGGMVLKLEQGENVFLQATDKNSLLGMEGANS
IFSGFLLFPDMEA*
.
PMID:28492532  



Database
Acc Id
Source(s)
ClinVar RCV002035005 CLINVAR
dbSNP (RS) rs1642591589 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene C1QB CLINVAR
OMIM 120570 CLINVAR