Version: 8.0.0
Date: Tue Jan 28 2025
25 results
Allele/Variant Genes: Mstn (Rno)

Mstnem1Cqin

(Rattus norvegicus)
Allele/Variant
Source: RGD:151347430
Genes: Mstn (Rno)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Mstnem2Mcwi

(Rattus norvegicus)
Allele/Variant
Source: RGD:5131949
Genes: Mstn (Rno)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

(mRatBN7.2)9:48455743C>G

(Rattus norvegicus)
Allele/Variant
Source: rs197255997
Genes: Mstn (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:48455743C>G

(mRatBN7.2)9:48458649A>T

(Rattus norvegicus)
Allele/Variant
Source: rs3321655524
Genes: Mstn (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:48458649A>T

Mstnem3Mcwi

(Rattus norvegicus)
Allele/Variant
Source: RGD:5131962
Genes: Mstn (Rno)
Synonyms: Not Available
Variant Type: deletion
Molecular Consequence: frameshift_variant
Diseases: Not Available
Variant Name: Not Available

Mstnem1Mcwi

(Rattus norvegicus)
Allele/Variant
Source: RGD:5143964
Genes: Mstn (Rno)
Synonyms: Not Available
Variant Type: deletion
Molecular Consequence: coding_sequence_variant, splice_acceptor_variant, intron_variant
Diseases: Not Available
Variant Name: Not Available

(mRatBN7.2)9:48456734C>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051344.1:g.48456734C>T
Genes: Mstn (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:48456734C>T

(mRatBN7.2)9:48458088G>A

(Rattus norvegicus)
Allele/Variant
Source: rs105871069
Genes: Mstn (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:48458088G>A

(mRatBN7.2)9:48457267G>A

(Rattus norvegicus)
Allele/Variant
Source: rs198159356
Genes: Mstn (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:48457267G>A

(mRatBN7.2)9:48458271A>G

(Rattus norvegicus)
Allele/Variant
Source: rs106284552
Genes: Mstn (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:48458271A>G

(mRatBN7.2)9:48455057G>A

(Rattus norvegicus)
Allele/Variant
Source: rs107263043
Genes: Mstn (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:48455057G>A

(mRatBN7.2)9:48455902T>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051344.1:g.48455902T>A
Genes: Mstn (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:48455902T>A

(mRatBN7.2)9:48457406C>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051344.1:g.48457406C>T
Genes: Mstn (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:48457406C>T

(mRatBN7.2)9:48458647C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3321618286
Genes: Mstn (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:48458647C>T

(mRatBN7.2)9:48455292G>A

(Rattus norvegicus)
Allele/Variant
Source: rs105337808
Genes: Mstn (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:48455292G>A

(mRatBN7.2)9:48453288A>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051344.1:g.48453288A>G
Genes: Mstn (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:48453288A>G

(mRatBN7.2)9:48454743C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3321677663
Genes: Mstn (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:48454743C>T

(mRatBN7.2)9:48457261A>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051344.1:g.48457261A>G
Genes: Mstn (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:48457261A>G

(mRatBN7.2)9:48453642T>C

(Rattus norvegicus)
Allele/Variant
Source: NC_051344.1:g.48453642T>C
Genes: Mstn (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:48453642T>C

(mRatBN7.2)9:48454443C>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051344.1:g.48454443C>A
Genes: Mstn (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:48454443C>A

(mRatBN7.2)9:48455545T>C

(Rattus norvegicus)
Allele/Variant
Source: rs105511398
Genes: Mstn (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:48455545T>C

(mRatBN7.2)9:48455547A>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051344.1:g.48455547A>G
Genes: Mstn (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:48455547A>G

(mRatBN7.2)9:48456704C>T

(Rattus norvegicus)
Allele/Variant
Source: rs105285630
Genes: Mstn (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:48456704C>T

(mRatBN7.2)9:48454897G>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051344.1:g.48454897G>A
Genes: Mstn (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:48454897G>A

(mRatBN7.2)9:48455021A>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051344.1:g.48455021A>G
Genes: Mstn (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:48455021A>G