Version: 8.0.0
Date: Tue Jan 28 2025
69 results
Allele/Variant Genes: H2-Ab1 (Mmu) Molecular Consequence: missense variant

H2-Ab1bm12

(Mus musculus)
Allele/Variant
Source: MGI:3586447
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: Not Available

(GRCm39)17:34483746T>G

(Mus musculus)
Allele/Variant
Source: rs249227964
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34483746T>G

(GRCm39)17:34483920A>T

(Mus musculus)
Allele/Variant
Source: rs581644025
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34483920A>T

(GRCm39)17:34483759G>T

(Mus musculus)
Allele/Variant
Source: rs215040960
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34483759G>T

(GRCm39)17:34483978C>T

(Mus musculus)
Allele/Variant
Source: rs108357614
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34483978C>T

(GRCm39)17:34483840A>T

(Mus musculus)
Allele/Variant
Source: rs107595512
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34483840A>T

(GRCm39)17:34483904G>C

(Mus musculus)
Allele/Variant
Source: rs586566512
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34483904G>C

(GRCm39)17:34483861A>T

(Mus musculus)
Allele/Variant
Source: rs583657844
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34483861A>T

(GRCm39)17:34483975G>T

(Mus musculus)
Allele/Variant
Source: rs230460846
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34483975G>T

(GRCm39)17:34483743G>T

(Mus musculus)
Allele/Variant
Source: rs583147738
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34483743G>T

(GRCm39)17:34483771T>A

(Mus musculus)
Allele/Variant
Source: rs216772183
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34483771T>A

(GRCm39)17:34483804C>A

(Mus musculus)
Allele/Variant
Source: rs262396542
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34483804C>A

(GRCm39)17:34483933C>A

(Mus musculus)
Allele/Variant
Source: rs216812224
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34483933C>A

(GRCm39)17:34486387G>A

(Mus musculus)
Allele/Variant
Source: rs48456922
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34486387G>A

(GRCm39)17:34483755A>C

(Mus musculus)
Allele/Variant
Source: rs585345427
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34483755A>C

(GRCm39)17:34483803A>G

(Mus musculus)
Allele/Variant
Source: rs585367375
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34483803A>G

(GRCm39)17:34483860C>T

(Mus musculus)
Allele/Variant
Source: rs108861703
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34483860C>T

(GRCm39)17:34483893G>C

(Mus musculus)
Allele/Variant
Source: rs233585078
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34483893G>C

(GRCm39)17:34483910C>G

(Mus musculus)
Allele/Variant
Source: rs227998502
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34483910C>G

(GRCm39)17:34482317C>T

(Mus musculus)
Allele/Variant
Source: rs107983435
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34482317C>T

(GRCm39)17:34486523G>A

(Mus musculus)
Allele/Variant
Source: rs230005216
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34486523G>A

(GRCm39)17:34483798A>C

(Mus musculus)
Allele/Variant
Source: rs221407800
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34483798A>C

(GRCm39)17:34483869G>C

(Mus musculus)
Allele/Variant
Source: rs586130970
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34483869G>C

(GRCm39)17:34483942A>C

(Mus musculus)
Allele/Variant
Source: rs229330097
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34483942A>C

(GRCm39)17:34486319A>G

(Mus musculus)
Allele/Variant
Source: rs46283069
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34486319A>G

(GRCm39)17:34483986C>A

(Mus musculus)
Allele/Variant
Source: rs240267920
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34483986C>A

(GRCm39)17:34483945T>C

(Mus musculus)
Allele/Variant
Source: rs216745465
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34483945T>C

(GRCm39)17:34483747A>C

(Mus musculus)
Allele/Variant
Source: rs259470336
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34483747A>C

(GRCm39)17:34482370G>A

(Mus musculus)
Allele/Variant
Source: rs108367066
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34482370G>A

(GRCm39)17:34483756T>A

(Mus musculus)
Allele/Variant
Source: rs232662853
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34483756T>A

(GRCm39)17:34483758G>A

(Mus musculus)
Allele/Variant
Source: rs255626592
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34483758G>A

(GRCm39)17:34486992C>T

(Mus musculus)
Allele/Variant
Source: rs243164767
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34486992C>T

(GRCm39)17:34483762A>T

(Mus musculus)
Allele/Variant
Source: rs243195174
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34483762A>T

(GRCm39)17:34483930G>A

(Mus musculus)
Allele/Variant
Source: rs584838136
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34483930G>A

(GRCm39)17:34483954T>C

(Mus musculus)
Allele/Variant
Source: rs238045072
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34483954T>C

(GRCm39)17:34483763G>C

(Mus musculus)
Allele/Variant
Source: rs578872933
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34483763G>C

(GRCm39)17:34483797T>C

(Mus musculus)
Allele/Variant
Source: rs251232353
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34483797T>C

(GRCm39)17:34483809T>A

(Mus musculus)
Allele/Variant
Source: rs220165475
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34483809T>A

(GRCm39)17:34483987A>C

(Mus musculus)
Allele/Variant
Source: rs107916351
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34483987A>C

(GRCm39)17:34483758G>C

(Mus musculus)
Allele/Variant
Source: rs255626592
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34483758G>C

(GRCm39)17:34483758G>T

(Mus musculus)
Allele/Variant
Source: rs255626592
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34483758G>T

(GRCm39)17:34483894C>T

(Mus musculus)
Allele/Variant
Source: rs579831517
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34483894C>T

(GRCm39)17:34483903G>T

(Mus musculus)
Allele/Variant
Source: rs583164817
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34483903G>T

(GRCm39)17:34483831A>G

(Mus musculus)
Allele/Variant
Source: rs244772792
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34483831A>G

(GRCm39)17:34482326T>G

(Mus musculus)
Allele/Variant
Source: rs108076422
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34482326T>G

(GRCm39)17:34483747A>T

(Mus musculus)
Allele/Variant
Source: rs259470336
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34483747A>T

(GRCm39)17:34483977C>G

(Mus musculus)
Allele/Variant
Source: rs107880552
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34483977C>G

(GRCm39)17:34484004C>T

(Mus musculus)
Allele/Variant
Source: rs222207961
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34484004C>T

(GRCm39)17:34482338T>C

(Mus musculus)
Allele/Variant
Source: rs108650860
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34482338T>C

(GRCm39)17:34486526G>A

(Mus musculus)
Allele/Variant
Source: rs221891211
Genes: H2-Ab1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34486526G>A