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

(mRatBN7.2)14:79832740T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3322609950
Genes: Nefh (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)14:79832740T>C

(mRatBN7.2)14:79834942T>G

(Rattus norvegicus)
Allele/Variant
Source: rs3322638860
Genes: Nefh (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)14:79834942T>G

(mRatBN7.2)14:79838077A>C

(Rattus norvegicus)
Allele/Variant
Source: rs3322677569
Genes: Nefh (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)14:79838077A>C

(mRatBN7.2)14:79838971G>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051349.1:g.79838971G>A
Genes: Nefh (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)14:79838971G>A

(mRatBN7.2)14:79832858A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3322632876
Genes: Nefh (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)14:79832858A>G

(mRatBN7.2)14:79832917C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3322712907
Genes: Nefh (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)14:79832917C>T

(mRatBN7.2)14:79835938T>G

(Rattus norvegicus)
Allele/Variant
Source: rs197287540
Genes: Nefh (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)14:79835938T>G

(mRatBN7.2)14:79838500C>T

(Rattus norvegicus)
Allele/Variant
Source: rs197360225
Genes: Nefh (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)14:79838500C>T

(mRatBN7.2)14:79839417G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3322677572
Genes: Nefh (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)14:79839417G>A

(mRatBN7.2)14:79833566C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3322612855
Genes: Nefh (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)14:79833566C>T

(mRatBN7.2)14:79831292A>G

(Rattus norvegicus)
Allele/Variant
Source: rs13453370
Genes: Nefh (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)14:79831292A>G

(mRatBN7.2)14:79833751G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3322632888
Genes: Nefh (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)14:79833751G>A

(mRatBN7.2)14:79837643A>G

(Rattus norvegicus)
Allele/Variant
Source: rs198512517
Genes: Nefh (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)14:79837643A>G

(mRatBN7.2)14:79831963A>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051349.1:g.79831963A>T
Genes: Nefh (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)14:79831963A>T

(mRatBN7.2)14:79831981T>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051349.1:g.79831981T>A
Genes: Nefh (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)14:79831981T>A

(mRatBN7.2)14:79833312G>A

(Rattus norvegicus)
Allele/Variant
Source: rs198678946
Genes: Nefh (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)14:79833312G>A

(mRatBN7.2)14:79837813A>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051349.1:g.79837813A>T
Genes: Nefh (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)14:79837813A>T

(mRatBN7.2)14:79837820T>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051349.1:g.79837820T>A
Genes: Nefh (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)14:79837820T>A

(mRatBN7.2)14:79832503G>T

(Rattus norvegicus)
Allele/Variant
Source: rs3322638849
Genes: Nefh (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)14:79832503G>T

(mRatBN7.2)14:79839708C>T

(Rattus norvegicus)
Allele/Variant
Source: rs198105226
Genes: Nefh (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)14:79839708C>T

(mRatBN7.2)14:79831076G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3322677464
Genes: Nefh (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)14:79831076G>A

(mRatBN7.2)14:79838737A>G

(Rattus norvegicus)
Allele/Variant
Source: rs198820847
Genes: Nefh (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)14:79838737A>G

(mRatBN7.2)14:79838761C>T

(Rattus norvegicus)
Allele/Variant
Source: rs197510653
Genes: Nefh (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)14:79838761C>T

(mRatBN7.2)14:79831116T>G

(Rattus norvegicus)
Allele/Variant
Source: rs13453933
Genes: Nefh (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)14:79831116T>G

(mRatBN7.2)14:79836803A>C

(Rattus norvegicus)
Allele/Variant
Source: rs3322677574
Genes: Nefh (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)14:79836803A>C

(mRatBN7.2)14:79839299G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3322572648
Genes: Nefh (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)14:79839299G>A

(mRatBN7.2)14:79830626G>A

(Rattus norvegicus)
Allele/Variant
Source: rs13449320
Genes: Nefh (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)14:79830626G>A

(mRatBN7.2)14:79836138G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3322661011
Genes: Nefh (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)14:79836138G>A

(mRatBN7.2)14:79832001G>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051349.1:g.79832001G>A
Genes: Nefh (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)14:79832001G>A

(mRatBN7.2)14:79839384A>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051349.1:g.79839384A>G
Genes: Nefh (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)14:79839384A>G

(mRatBN7.2)14:79835373A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3322275267
Genes: Nefh (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)14:79835373A>G

(mRatBN7.2)14:79838646G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3322712870
Genes: Nefh (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)14:79838646G>A

(mRatBN7.2)14:79832336A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3322638915
Genes: Nefh (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)14:79832336A>G

(mRatBN7.2)14:79835721A>T

(Rattus norvegicus)
Allele/Variant
Source: rs3322712898
Genes: Nefh (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)14:79835721A>T

(mRatBN7.2)14:79838610C>T

(Rattus norvegicus)
Allele/Variant
Source: rs198905248
Genes: Nefh (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)14:79838610C>T