Version: 8.0.0
Date: Tue Jan 28 2025
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All
All
Gene
Gene Ontology
Disease
Allele/Variant
Model
HTP Dataset Index
Allele/Variant
Show all Categories
Species
Rattus norvegicus
31
×
Category
variant
31
×
Variant Type
SNP
31
×
Molecular Consequence
intron variant
26
×
synonymous variant
3
×
3 prime UTR variant
2
×
Genes
C1qb (Rno)
31
×
Filter
31
results
Page 1 of 1
Allele/Variant
Genes: C1qb (Rno)
(mRatBN7.2)5:149119981A>G
(
Rattus norvegicus
)
Allele/Variant
Source:
NC_051340.1:g.149119981A>G
Genes:
C1qb (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)5:149119981A>G
(mRatBN7.2)5:149120490A>G
(
Rattus norvegicus
)
Allele/Variant
Source:
NC_051340.1:g.149120490A>G
Genes:
C1qb (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)5:149120490A>G
(mRatBN7.2)5:149120731T>C
(
Rattus norvegicus
)
Allele/Variant
Source:
NC_051340.1:g.149120731T>C
Genes:
C1qb (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)5:149120731T>C
(mRatBN7.2)5:149121386A>G
(
Rattus norvegicus
)
Allele/Variant
Source:
NC_051340.1:g.149121386A>G
Genes:
C1qb (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)5:149121386A>G
(mRatBN7.2)5:149121433T>C
(
Rattus norvegicus
)
Allele/Variant
Source:
NC_051340.1:g.149121433T>C
Genes:
C1qb (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)5:149121433T>C
(mRatBN7.2)5:149122309C>T
(
Rattus norvegicus
)
Allele/Variant
Source:
rs197619401
Genes:
C1qb (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)5:149122309C>T
(mRatBN7.2)5:149122875A>G
(
Rattus norvegicus
)
Allele/Variant
Source:
NC_051340.1:g.149122875A>G
Genes:
C1qb (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)5:149122875A>G
(mRatBN7.2)5:149122923T>C
(
Rattus norvegicus
)
Allele/Variant
Source:
NC_051340.1:g.149122923T>C
Genes:
C1qb (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)5:149122923T>C
(mRatBN7.2)5:149122993A>G
(
Rattus norvegicus
)
Allele/Variant
Source:
NC_051340.1:g.149122993A>G
Genes:
C1qb (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)5:149122993A>G
(mRatBN7.2)5:149120063A>G
(
Rattus norvegicus
)
Allele/Variant
Source:
rs197607164
Genes:
C1qb (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)5:149120063A>G
(mRatBN7.2)5:149120416T>C
(
Rattus norvegicus
)
Allele/Variant
Source:
rs3320730767
Genes:
C1qb (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)5:149120416T>C
(mRatBN7.2)5:149122596G>A
(
Rattus norvegicus
)
Allele/Variant
Source:
NC_051340.1:g.149122596G>A
Genes:
C1qb (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)5:149122596G>A
(mRatBN7.2)5:149119358G>A
(
Rattus norvegicus
)
Allele/Variant
Source:
rs8148278
Genes:
C1qb (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
synonymous_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)5:149119358G>A
(mRatBN7.2)5:149121658A>G
(
Rattus norvegicus
)
Allele/Variant
Source:
NC_051340.1:g.149121658A>G
Genes:
C1qb (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)5:149121658A>G
(mRatBN7.2)5:149124031C>T
(
Rattus norvegicus
)
Allele/Variant
Source:
rs198263679
Genes:
C1qb (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)5:149124031C>T
(mRatBN7.2)5:149118887G>T
(
Rattus norvegicus
)
Allele/Variant
Source:
NC_051340.1:g.149118887G>T
Genes:
C1qb (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
3_prime_UTR_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)5:149118887G>T
(mRatBN7.2)5:149120576G>A
(
Rattus norvegicus
)
Allele/Variant
Source:
NC_051340.1:g.149120576G>A
Genes:
C1qb (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)5:149120576G>A
(mRatBN7.2)5:149120608G>A
(
Rattus norvegicus
)
Allele/Variant
Source:
NC_051340.1:g.149120608G>A
Genes:
C1qb (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)5:149120608G>A
(mRatBN7.2)5:149120790G>A
(
Rattus norvegicus
)
Allele/Variant
Source:
rs3323565835
Genes:
C1qb (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)5:149120790G>A
(mRatBN7.2)5:149121245C>T
(
Rattus norvegicus
)
Allele/Variant
Source:
rs197179332
Genes:
C1qb (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)5:149121245C>T
(mRatBN7.2)5:149121560G>C
(
Rattus norvegicus
)
Allele/Variant
Source:
NC_051340.1:g.149121560G>C
Genes:
C1qb (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)5:149121560G>C
(mRatBN7.2)5:149121700C>G
(
Rattus norvegicus
)
Allele/Variant
Source:
rs105983715
Genes:
C1qb (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)5:149121700C>G
(mRatBN7.2)5:149123262C>T
(
Rattus norvegicus
)
Allele/Variant
Source:
rs199122229
Genes:
C1qb (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)5:149123262C>T
(mRatBN7.2)5:149124021G>C
(
Rattus norvegicus
)
Allele/Variant
Source:
rs196971341
Genes:
C1qb (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)5:149124021G>C
(mRatBN7.2)5:149118843C>T
(
Rattus norvegicus
)
Allele/Variant
Source:
rs8146070
Genes:
C1qb (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
3_prime_UTR_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)5:149118843C>T
(mRatBN7.2)5:149119331A>G
(
Rattus norvegicus
)
Allele/Variant
Source:
rs8162791
Genes:
C1qb (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
synonymous_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)5:149119331A>G
(mRatBN7.2)5:149119439G>A
(
Rattus norvegicus
)
Allele/Variant
Source:
NC_051340.1:g.149119439G>A
Genes:
C1qb (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
synonymous_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)5:149119439G>A
(mRatBN7.2)5:149119790C>T
(
Rattus norvegicus
)
Allele/Variant
Source:
NC_051340.1:g.149119790C>T
Genes:
C1qb (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)5:149119790C>T
(mRatBN7.2)5:149119901C>T
(
Rattus norvegicus
)
Allele/Variant
Source:
NC_051340.1:g.149119901C>T
Genes:
C1qb (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)5:149119901C>T
(mRatBN7.2)5:149120292T>C
(
Rattus norvegicus
)
Allele/Variant
Source:
rs198461354
Genes:
C1qb (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)5:149120292T>C
(mRatBN7.2)5:149120342G>A
(
Rattus norvegicus
)
Allele/Variant
Source:
NC_051340.1:g.149120342G>A
Genes:
C1qb (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)5:149120342G>A
Page 1 of 1
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